14 Researchers jobs in Quebec

ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate.
ICON plc est une organisation de premier plan spécialisée en intelligence en santé et en recherche clinique. Nous sommes fiers de favoriser un environnement inclusif qui stimule l'innovation et l'excellence. Nous vous invitons à vous joindre à nous dans notre mission visant à façonner l'avenir du développement clinique en tant qu'Associé(e) de recherche clinique.
**What you will be doing:**
+ Oversee multiple oncology trials, ensuring high-quality execution
+ Provide leadership and mentorship to junior flex team members
+ Act as Lead SM, training and guiding other Site Managers on study protocols
+ Develop essential study start-up documents, including SIV agendas
+ Represent Site Managers and Lead Trial Managers (LTMs) in key meetings
+ Ensure the SM perspective is reflected in study documents like Monitoring Guidelines
+ Review reports (SQV, SMV, SCV) for sites assigned to other SMs within the same trial
+ Support country budget development and contract negotiations in collaboration with CCS colleagues
+ Assist with ASV activities and ensure alignment with study objectives
+ Maintain compliance with Metrics/KPIs as outlined in the Quality Oversight Plan (QOP)
**Ce que vous ferez :**
+ Superviser plusieurs essais en oncologie, en veillant à leur exécution de haute qualité
+ Fournir du leadership et du mentorat aux membres juniors de l'équipe flexible
+ Agir en tant que Gestionnaire de Site principal (Lead SM), en formant et guidant les autres Gestionnaires de Site sur les protocoles d'étude
+ Développer des documents essentiels pour le démarrage des études, y compris les ordres du jour des visites de mise en place des sites (SIV)
+ Représenter les Gestionnaires de Site et les Gestionnaires d'Essai Principaux (LTMs) lors de réunions clés
+ S'assurer que la perspective des Gestionnaires de Site est bien reflétée dans les documents d'étude, comme les Lignes directrices de Surveillance
+ Réviser les rapports (SQV, SMV, SCV) pour les sites attribués à d'autres Gestionnaires de Site dans le même essai
+ Soutenir le développement des budgets pays et les négociations contractuelles en collaboration avec les collègues du CCS
+ Assister aux activités ASV et veiller à l'alignement avec les objectifs de l'étude
+ Maintenir la conformité aux indicateurs de performance (Metrics/KPIs) conformément au Plan de Surveillance de la Qualité (QOP)
**You Are:**
+ Remote position located in Montreal
+ Bilingual - Proficient in both written and spoken French and English.
+ Minimum of a B.Sc., R.N., or equivalent degree, preferably in Biological Sciences
+ At least 2 years of experience monitoring clinical trials in the pharmaceutical industry
+ Experience in multiple therapeutic areas is an asset, particularly in oncology (Hematology, Prostate Cancer, Lung Cancer, Early Development - Phase 1)
+ Knowledge of risk-based/analytical monitoring approaches is an asset
+ Proficiency in clinical trial systems such as CTMS, EDC, TMF, IWRS, and safety reporting tools
+ Ability to actively drive patient recruitment strategies at assigned sites
+ Strong collaboration with investigators and site staff to meet study timelines
+ Effective communication and influencing skills to manage study sites effectively, both remotely and in-person
+ Ability to work independently while being a strong collaborator
+ In-depth understanding of Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements
+ Up to 50% regional travel required
**Vous êtes :**
+ Poste en télétravail basé à Montréal
+ Bilingue - Maîtrise du français et de l'anglais, à l'écrit comme à l'oral
+ Titulaire d'un B.Sc., d'un diplôme d'infirmier(ère) autorisé(e) (R.N.), ou d'un diplôme équivalent, de préférence en sciences biologiques
+ Minimum de 2 ans d'expérience en surveillance d'essais cliniques dans l'industrie pharmaceutique
+ Expérience dans plusieurs aires thérapeutiques, un atout - particulièrement en oncologie (hématologie, cancer de la prostate, cancer du poumon, développement précoce - phase 1)
+ Connaissance des approches de surveillance analytique/basée sur les risques, un atout
+ Maîtrise des systèmes d'essais cliniques : CTMS, EDC, TMF, IWRS et outils de déclaration de sécurité
+ Capacité à piloter activement les stratégies de recrutement de patients sur les sites assignés
+ Forte collaboration avec les investigateurs et le personnel des sites pour respecter les échéanciers de l'étude
+ Excellentes compétences en communication et en influence pour gérer efficacement les sites d'étude, à distance et en présentiel
+ Capacité à travailler de manière autonome tout en favorisant une collaboration efficace
+ Connaissance approfondie des Bonnes Pratiques Cliniques (BPC), des lignes directrices ICH et des exigences réglementaires locales
+ Disponibilité pour voyager jusqu'à 50 % dans la région
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs
+ Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
+ Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.

Job Description

Job Description

Join the Team!

Are you ready to take on exciting challenges in a dynamic and fast-paced environment? At NanoXplore, we offer an opportunity to be part of a rapidly growing company that is at the forefront of creating sustainable products, pushing the boundaries of innovation across multiple industries.

We believe in fostering creativity and encouraging fresh ideas-whether big or small-because innovation is at the heart of everything we do. Joining our team means you'll have the chance to contribute to groundbreaking solutions, collaborate with talented professionals, and make a real impact on a global scale.

If you're looking to grow, innovate, and make a difference, NanoXplore is the place for you!

Summary Of The Role

Lead and support research and development activities focused on thermoplastics and polymer composites, while also providing technical expertise to the Sales Team. The role bridges internal R&D efforts with customer-facing initiatives by managing customer projects, supporting business development, and ensuring effective collaboration between labs, external partners, and customers.

Key Responsabilities

• Lead technical activities and manage the day-to-day operations of assigned R&D projects;
• Plan and execute tasks to ensure timely progress toward the goals of R&D and Sales-related projects and programs;
• Provide technical support to the Sales and Marketing teams;
• Participate in customer meetings to offer technical support and develop project proposals aligned with customer needs;
• Contribute to internal and external meetings, seminars, and discussions related to R&D and Sales initiatives;
• Prepare and deliver progress reports on R&D activities; support the R&D Manager in drafting program updates and documentation;
• Maintain up-to-date knowledge and technical expertise in relevant fields;
• Develop design of experiments for new R&D projects in collaboration with customers, partners, and collaborators, subject to written approval from R&D managers;
• Ensure compliance with company policies, methodologies, and project standards;
• Identify and communicate potential risks or challenges related to R&D projects to R&D managers.

Qualifications

• Master or PhD in materials/polymers engineering or chemical/mechanical engineering or related fields;
• Strong background in plastics, polymer resins, and advanced materials, with the ability to leverage this expertise to identify business opportunities, support sales, and solve industrial technical challenges;
• Solid understanding of polymer fundamentals (both thermosets and thermoplastics) and related performance requirements, as well as familiarity with polymer processing equipment;
• Practical knowledge of the application of polymer fillers, stabilizers, and additives;
• Proven experimental expertise in understanding and applying polymer structure-property relationships.

Skills & Attitude

• Strong organizational skills with the ability to manage multiple tasks and priorities effectively;
• Proven ability to define problems, collect and analyze data, and draw valid conclusions;
• Excellent time management and clear, effective communication skills;
• Reliable and dependable;
• Creative in developing technical solutions;
• Hardworking and committed;
• Adaptable to shifting priorities and organizational changes;
• Maintains a positive, proactive attitude;
• Strong interpersonal skills;
• Team-oriented, able to contribute effectively to fast-paced projects.

At NanoXplore, we value our employees and offer a comprehensive benefits package to support your well-being:

• RRSP/DPSP program;
• Group insurance program including medical and dental coverage;
• Telemedicine program for you and your immediate family;
• Employee and family assistance program;
• Free on-site gym;
• Regularly organized social events (potluck, BBQ and more).

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What will you be doing?

• Works on multiple trials within Oncology
• Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes
• Mentors/coaches junior flex team
• Acts as Lead SM-training other SMs on study
• Develops site start up documents for studies including SIV agenda
• Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
• Represents LTMs or SMs on SMTs/meetings
• Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
• Supports country budget development and/or contract negotiation in liaison with CCS colleagues
• Assists with ASV
• Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

Interfaces – Primary/Other

• Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials.
• Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.)

What do you need to have?

• Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
• Must be located in Canada
• Will work on US remote monitoring only
• Have a minimum of 2-5 years’ experience in monitoring pharmaceutical industry clinical trials
• Have a minimum of 1-2 years' experience monitoring Oncology trials
• Knowledge of several therapeutic areas
• Analytical/risk-based monitoring experience is an asset
• Ability to actively drive patient recruitment strategies at assigned sites
• Ability to partner closely with investigator and site staff to meet all of our study timelines
• Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).
• Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.
• Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
• To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON:

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What will you be doing?

• Works on multiple trials within Oncology
• Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes
• Mentors/coaches junior flex team
• Acts as Lead SM-training other SMs on study
• Develops site start up documents for studies including SIV agenda
• Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
• Represents LTMs or SMs on SMTs/meetings
• Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
• Supports country budget development and/or contract negotiation in liaison with CCS colleagues
• Assists with ASV
• Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

Interfaces – Primary/Other

• Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials.
• Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.)

What do you need to have?

• Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
• Must be located in Canada
• Will work on US remote monitoring only
• Have a minimum of 2-5 years’ experience in monitoring pharmaceutical industry clinical trials
• Have a minimum of 1-2 years' experience monitoring Oncology trials
• Knowledge of several therapeutic areas
• Analytical/risk-based monitoring experience is an asset
• Ability to actively drive patient recruitment strategies at assigned sites
• Ability to partner closely with investigator and site staff to meet all of our study timelines
• Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).
• Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.
• Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
• To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON:

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What will you be doing?

• Works on multiple trials within Oncology
• Demonstrated leadership, through involvement in specific initiatives when needed, and/or SME to systems and/or processes
• Mentors/coaches junior flex team
• Acts as Lead SM-training other SMs on study
• Develops site start up documents for studies including SIV agenda
• Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
• Represents LTMs or SMs on SMTs/meetings
• Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
• Supports country budget development and/or contract negotiation in liaison with CCS colleagues
• Assists with ASV
• Metrics/KPIs: Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

Interfaces – Primary/Other

• Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials.
• Other Interfaces: Study Responsible Physician, Regional Quality and Compliance. Manager/Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.)

What do you need to have?

• Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
• Must be located in Canada
• Will work on US remote monitoring only
• Have a minimum of 2-5 years’ experience in monitoring pharmaceutical industry clinical trials
• Have a minimum of 1-2 years' experience monitoring Oncology trials
• Knowledge of several therapeutic areas
• Analytical/risk-based monitoring experience is an asset
• Ability to actively drive patient recruitment strategies at assigned sites
• Ability to partner closely with investigator and site staff to meet all of our study timelines
• Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).
• Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.
• Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
• To qualify, applicants must be legally authorized to work in Canada, and should not require, now or in the future, sponsorship for employment visa status.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON:

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

IQVIA est à la recherche d'un associé de recherche clinique II avec une expérience en surveillance en oncologie basé dans l'Est du Canada. Doit être bilingue en français et en anglais.
**Aperçu du poste**
Surveiller et gérer les centres pour s'assurer qu'ils réalisent les études et produisent des rapports sur les données d'étude conformément au protocole d'étude, aux règlements et aux lignes directrices applicables, et aux exigences du promoteur.
**Fonctions essentielles**
+ Effectuer des visites de surveillance du centre (visites de sélection, d'initiation, de surveillance et de clôture) conformément à la portée des travaux indiquée au contrat et aux bonnes pratiques cliniques.
+ Travailler avec les centres pour adapter, piloter et suivre le plan de recrutement des sujets conformément aux besoins du projet afin d'améliorer la prévisibilité.
+ Administrer le protocole et la formation sur les études connexe dans les centres assignés et établir régulièrement la communication avec les centres pour gérer les attentes et les problèmes en cours de projet.
+ Évaluer la qualité et l'intégrité des pratiques du centre d'étude liées au bon déroulement du protocole et au respect de la réglementation applicable. Signaler les problèmes de qualité, le cas échéant.
+ Gérer l'avancement des études assignées en suivant les soumissions et les approbations réglementaires, le recrutement et l'inscription, l'achèvement et la soumission du cahier d'observation (CRF), ainsi que la production et la résolution des requêtes de données. Apporter son appui pendant la phase de démarrage, au besoin.
+ S'assurer que les copies/originaux (selon les besoins) des documents du centre sont ajoutés au dossier principal d'essai (DPE) et vérifier que le dossier du centre de l'investigateur (DCI) est conservé conformément aux BPC et aux exigences réglementaires locales.
+ Créer et maintenir une documentation appropriée concernant la gestion du centre, les résultats des visites de surveillance et les plans d'action en soumettant des rapports de visite réguliers, en générant des lettres de suivi et d'autres documents d'étude requis.
+ Collaborer et assurer la liaison avec les membres de l'équipe de l'étude pour le soutien à l'exécution du projet, le cas échéant.
+ Le cas échéant, soutenir l'élaboration du plan de recrutement des sujets du projet pour un centre donné.
+ Le cas échéant, superviser la gestion financière du centre conformément à l'accord d'essai clinique signé et récupérer les factures conformément aux exigences locales.
**Diplômes et expérience**
+ Baccalauréat dans une discipline scientifique ou en soins de santé exigé
+ Au moins 2?ans d'expérience en surveillance sur place.
+ Une combinaison équivalente d'études, de formation et d'expérience peut aussi être acceptée.
+ Bonne connaissance et aptitude à appliquer les exigences réglementaires applicables en matière de recherche clinique.
+ C'est-à-dire les lignes directrices des bonnes pratiques cliniques (BPC) et du Conseil international d'harmonisation (CIH).
+ Bonne connaissance des thérapies et protocoles, tels que présentés dans la formation en entreprise.
+ Compétences informatiques, y compris la maîtrise de Microsoft Word, Excel et PowerPoint et de l'utilisation d'un ordinateur portable ainsi que d'un iPhone et d'un iPad (le cas échéant).
+ Maîtrise écrite et verbale de l'anglais et du français
+ Solides compétences en matière d'organisation et de résolution de problèmes.
+ Gestion efficace du temps et des finances.
+ Capacité à établir et à entretenir des relations de travail efficaces avec les collègues, les gestionnaires et les clients.
+ Vous devrez soutenir, assurer la liaison avec et/ou travailler avec des (clients et/ou fournisseurs) d'IQVIA partout au Canada et à travers le monde, par conséquent, une connaissance fonctionnelle de l'anglais, tant à l'écrit qu'à l'oral, est nécessaire à l'exercice des fonctions de ce poste.
___
English:
IQVIA is seeking a Clinical Research Associate II with Oncology monitoring experience based in Eastern Canada. Must be bilingual in French and English.
**BASIC FUNCTIONS:**
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA t0 ensure all monitoring activities are conducted according to study requirements. This position may also serve as Lead CRA.
**II ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:**
+ Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
+ Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
+ Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
+ Trains site staff on the EDC system and verifies site computer system.
+ Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISSC.
+ Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
+ Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required.
+ Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries.
+ Perform SAE review and reconciliation
+ May review protocols, eCRFs, study manuals and other related documents, as requested by Clinical Trial Manager and/or Lead CRA.
+ Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
+ Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
+ May assist with, and attend, Investigator Meetings for assigned studies.
+ Attends study-related, company, departmental, and external meetings, as required.
+ May serve as mentor for new clinical study monitors.
+ Authorized to request site audits due to data integrity concerns.
+ Ensure internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
+ Ensure all study deliverables are completed per IQVIA Biotech and study timelines.
**LEAD CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:**
The Lead Clinical Research Associate **may** perform any of the following tasks:
+ Participate in the investigator recruitment process. Perform site evaluation visits, as needed, of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
+ Collaborate with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
+ Perform study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
+ Assists with, and attends, Investigator Meetings for assigned studies.
+ Train site staff on the EDC system and verify site computer system.
+ Assist in resolving any issues to ensure compliance with site file audits in conjunction with ISSC.
+ Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
+ Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required.
+ Review the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Work with sites to resolve data queries.
+ May review draft protocols, eCRFs, monitoring reports and follow-up letters, study manuals and other prepare study-related documents and templates, as requested by the CTM and/or PM.
+ May serve as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
+ Assist CTM and/or PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions.
+ Assist the study management in identifying and generating changes in scope
+ Perform study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
+ Authorized to request site audits due to data integrity concerns.
+ Attend study-related, company, departmental, and external meetings, as required.
+ Ensure internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
+ Ensure all study deliverables are completed per IQVIA Biotech and study timelines
+ Conduct Field Evaluation Visits and field training of CRA Is, IIs and Sr CRAs.
+ Serve as mentor for junior CRAs and those new to the company and/or study.
+ Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA.
+ Review and approve CRA travel expenses and time sheets.
+ Perform other duties, as requested.
**KNOWLEDGE, SKILLS AND ABILITIES:**
+ Knowledge of clinical research process and medical terminology.
+ Strong written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
+ Good organizational and interpersonal skills.
+ Ability to reason independently and recommend specific solutions in clinical settings.
+ Ability to understand electronic data capture including basic data processing functions.
+ Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
+ Ability to qualify for a major credit card, rent an automobile
**PHYSICAL REQUIREMENTS:**
+ Very limited physical effort required to perform normal job duties
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech
+ Extensive use of keyboard requiring repetitive motion of fingers
+ Regular sitting for extended periods of time
**MINIMUM RECRUITMENT STANDARDS:**
+ BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc.) and a minimum of two (2) years of monitoring/site management experience is required; or an equivalent combination of education, training and experience.
+ Must possess 2+ years of oncology and/or medical device experience.
+ Experience in monitoring and/or coordinating clinical trials required.
+ Must be able to travel domestically approximately 65%-85%.
+ Valid driver's license
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
+ You will be required to support, liaise with and/or work with IQVIA customers and/or suppliers across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position.
Comme nos équipes de recrutement sont mondiales, veuillez soumettre votre CV en anglais et en français.
As our hiring teams are global, please submit your resume in both English and French.
IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez est fière d'être un employeur souscrivant au principe de l'égalité d'accès à l'emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l'orientation sexuelle, l'identité de genre, l'origine nationale, le handicap, l'âge, l'état matrimonial ou tout autre statut protégé par la loi applicable. Des mesures d'adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d'adaptation, nous vous encourageons à contacter notre équipe d'acquisition de talents au , afin qu'IQVIA puisse soutenir votre participation au processus de recrutement.
Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: , so that IQVIA can support your participation in the recruitment process.
Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

? **French:** Pour être éligible à ce poste, vous devez résider dans le même pays où se trouve le poste.
IQVIA Biotech est à la recherche d'un associé de recherche clinique II avec une expérience en surveillance en oncologie basé dans l'Est du Canada. Doit être bilingue en français et en anglais.
**Aperçu du poste**
Surveiller et gérer les centres pour s'assurer qu'ils réalisent les études et produisent des rapports sur les données d'étude conformément au protocole d'étude, aux règlements et aux lignes directrices applicables, et aux exigences du promoteur.
**Fonctions essentielles**
+ Effectuer des visites de surveillance du centre (visites de sélection, d'initiation, de surveillance et de clôture) conformément à la portée des travaux indiquée au contrat et aux bonnes pratiques cliniques.
+ Travailler avec les centres pour adapter, piloter et suivre le plan de recrutement des sujets conformément aux besoins du projet afin d'améliorer la prévisibilité.
+ Administrer le protocole et la formation sur les études connexe dans les centres assignés et établir régulièrement la communication avec les centres pour gérer les attentes et les problèmes en cours de projet.
+ Évaluer la qualité et l'intégrité des pratiques du centre d'étude liées au bon déroulement du protocole et au respect de la réglementation applicable. Signaler les problèmes de qualité, le cas échéant.
+ Gérer l'avancement des études assignées en suivant les soumissions et les approbations réglementaires, le recrutement et l'inscription, l'achèvement et la soumission du cahier d'observation (CRF), ainsi que la production et la résolution des requêtes de données. Apporter son appui pendant la phase de démarrage, au besoin.
+ S'assurer que les copies/originaux (selon les besoins) des documents du centre sont ajoutés au dossier principal d'essai (DPE) et vérifier que le dossier du centre de l'investigateur (DCI) est conservé conformément aux BPC et aux exigences réglementaires locales.
+ Créer et maintenir une documentation appropriée concernant la gestion du centre, les résultats des visites de surveillance et les plans d'action en soumettant des rapports de visite réguliers, en générant des lettres de suivi et d'autres documents d'étude requis.
+ Collaborer et assurer la liaison avec les membres de l'équipe de l'étude pour le soutien à l'exécution du projet, le cas échéant.
+ Le cas échéant, soutenir l'élaboration du plan de recrutement des sujets du projet pour un centre donné.
+ Le cas échéant, superviser la gestion financière du centre conformément à l'accord d'essai clinique signé et récupérer les factures conformément aux exigences locales.
**Diplômes et expérience**
+ Baccalauréat dans une discipline scientifique ou en soins de santé exigé
+ Au moins 2?ans d'expérience en surveillance sur place.
+ Une combinaison équivalente d'études, de formation et d'expérience peut aussi être acceptée.
+ Bonne connaissance et aptitude à appliquer les exigences réglementaires applicables en matière de recherche clinique.
+ C'est-à-dire les lignes directrices des bonnes pratiques cliniques (BPC) et du Conseil international d'harmonisation (CIH).
+ Bonne connaissance des thérapies et protocoles, tels que présentés dans la formation en entreprise.
+ Compétences informatiques, y compris la maîtrise de Microsoft Word, Excel et PowerPoint et de l'utilisation d'un ordinateur portable ainsi que d'un iPhone et d'un iPad (le cas échéant).
+ Maîtrise écrite et verbale de l'anglais et du français
+ Solides compétences en matière d'organisation et de résolution de problèmes.
+ Gestion efficace du temps et des finances.
+ Capacité à établir et à entretenir des relations de travail efficaces avec les collègues, les gestionnaires et les clients.
+ Vous devrez soutenir, assurer la liaison avec et/ou travailler avec des (clients et/ou fournisseurs) d'IQVIA partout au Canada et à travers le monde, par conséquent, une connaissance fonctionnelle de l'anglais, tant à l'écrit qu'à l'oral, est nécessaire à l'exercice des fonctions de ce poste.
___
**English:** To be eligible for this position, you must reside in the same country where the job is located.
IQVIA Biotech is seeking a Clinical Research Associate II with Oncology monitoring experience based in Eastern Canada. Must be bilingual in French and English.
**BASIC FUNCTIONS:**
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA t0 ensure all monitoring activities are conducted according to study requirements. This position may also serve as Lead CRA.
**II ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:**
+ Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
+ Collaborates with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
+ Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
+ Trains site staff on the EDC system and verifies site computer system.
+ Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISSC.
+ Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
+ Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required.
+ Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries.
+ Perform SAE review and reconciliation
+ May review protocols, eCRFs, study manuals and other related documents, as requested by Clinical Trial Manager and/or Lead CRA.
+ Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
+ Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
+ May assist with, and attend, Investigator Meetings for assigned studies.
+ Attends study-related, company, departmental, and external meetings, as required.
+ May serve as mentor for new clinical study monitors.
+ Authorized to request site audits due to data integrity concerns.
+ Ensure internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
+ Ensure all study deliverables are completed per IQVIA Biotech and study timelines.
**LEAD CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:**
The Lead Clinical Research Associate **may** perform any of the following tasks:
+ Participate in the investigator recruitment process. Perform site evaluation visits, as needed, of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
+ Collaborate with the ISSC department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISSC and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
+ Perform study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
+ Assists with, and attends, Investigator Meetings for assigned studies.
+ Train site staff on the EDC system and verify site computer system.
+ Assist in resolving any issues to ensure compliance with site file audits in conjunction with ISSC.
+ Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
+ Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required.
+ Review the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Work with sites to resolve data queries.
+ May review draft protocols, eCRFs, monitoring reports and follow-up letters, study manuals and other prepare study-related documents and templates, as requested by the CTM and/or PM.
+ May serve as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
+ Assist CTM and/or PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions.
+ Assist the study management in identifying and generating changes in scope
+ Perform study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
+ Authorized to request site audits due to data integrity concerns.
+ Attend study-related, company, departmental, and external meetings, as required.
+ Ensure internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
+ Ensure all study deliverables are completed per IQVIA Biotech and study timelines
+ Conduct Field Evaluation Visits and field training of CRA Is, IIs and Sr CRAs.
+ Serve as mentor for junior CRAs and those new to the company and/or study.
+ Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA.
+ Review and approve CRA travel expenses and time sheets.
+ Perform other duties, as requested.
**KNOWLEDGE, SKILLS AND ABILITIES:**
+ Knowledge of clinical research process and medical terminology.
+ Strong written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
+ Good organizational and interpersonal skills.
+ Ability to reason independently and recommend specific solutions in clinical settings.
+ Ability to understand electronic data capture including basic data processing functions.
+ Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
+ Ability to qualify for a major credit card, rent an automobile
**PHYSICAL REQUIREMENTS:**
+ Very limited physical effort required to perform normal job duties
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech
+ Extensive use of keyboard requiring repetitive motion of fingers
+ Regular sitting for extended periods of time
**MINIMUM RECRUITMENT STANDARDS:**
+ BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc.) and a minimum of two (2) years of monitoring/site management experience is required; or an equivalent combination of education, training and experience.
+ Must possess 2+ years of oncology and/or medical device experience.
+ Experience in monitoring and/or coordinating clinical trials required.
+ Must be able to travel domestically approximately 65%-85%.
+ Valid driver's license
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer
+ You will be required to support, liaise with and/or work with IQVIA customers and/or suppliers across Canada and around the world therefore, a functional knowledge of English, both written and spoken, is necessary to perform the duties of this position.
Comme nos équipes de recrutement sont mondiales, veuillez soumettre votre CV en anglais et en français.
As our hiring teams are global, please submit your resume in both English and French.
IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé. IQVIA se consacre à accélérer le développement et la commercialisation de traitements médicaux innovants pour aider à améliorer les résultats des patients et la santé de la population dans le monde entier. Pour en savoir plus, visitez est fière d'être un employeur souscrivant au principe de l'égalité d'accès à l'emploi. Tous les candidats qualifiés seront pris en considération pour un emploi sans égard à la race, la couleur, la religion, le sexe, l'orientation sexuelle, l'identité de genre, l'origine nationale, le handicap, l'âge, l'état matrimonial ou tout autre statut protégé par la loi applicable. Des mesures d'adaptation pour les candidats handicapés sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui nécessite une mesure d'adaptation, nous vous encourageons à contacter notre équipe d'acquisition de talents au , afin qu'IQVIA puisse soutenir votre participation au processus de recrutement.
Veuillez noter qu'il est possible que nous utilisions l'intelligence artificielle (IA) dans le traitement de votre candidature. Cependant, nous utilisons l'IA uniquement pour aider notre équipe de recrutement à sélectionner ou à évaluer les candidatures, et non pas pour remplacer la prise des décisions par les membres de notre équipe.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: , so that IQVIA can support your participation in the recruitment process.
Please note that we may use artificial intelligence (AI) in the processing of your application. However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

Job Description

Job Description

Job Title: Applied AI Research Scientist
Location: Montreal, Canada (Hybrid)
Employment Type: Full-time
Experience Level: Mid-Senior Level
Industry: Artificial Intelligence / Computer Vision
Job Sourced By: Industry Professional sourcing candidates for its client based in Canada

About the Role

Our client, a leading innovator in AI and Computer Vision, is seeking an Applied AI Research Scientist to join their Montreal-based Research & Technology team. This hybrid role offers an exciting opportunity to contribute to cutting-edge innovation in a multidisciplinary environment. The ideal candidate is a highly motivated, creative thinker with strong technical expertise, passionate about developing novel AI methodologies and transforming them into scalable, real-world applications.

Requirements

• Ph.D. or Masters degree in Computer Science, Electrical Engineering, or a related field with a focus on AI, machine/deep learning, or computer vision.

• 25 years of relevant research experience in robotics, autonomous systems, or related domains.

• Strong theoretical knowledge of supervised, unsupervised, self-supervised, few-shot, and zero-shot learning techniques.

• Hands-on experience developing and deploying computer vision models in academic or industrial settings.

• Solid understanding of image sensing modalities such as RGB, RADAR, Infrared, LIDAR, hyperspectral, thermal, etc.

• Expertise in deep learning architectures including CNNs, Transformers, and foundation models for tasks like detection, segmentation, and recognition.

• Proficient in Python and C++ with practical experience using ML/DL frameworks such as PyTorch, TensorFlow, Scikit-learn, and OpenCV.

• Demonstrated ability to design experiments, analyze data, and optimize models for performance.

• Strong written and verbal communication skills in English, with the ability to clearly convey complex technical concepts.

• Demonstrated ability to publish research in leading AI and computer vision conferences/journals (e.g., NeurIPS, CVPR, ICCV, ECCV, AAAI, PAMI).

• Excellent collaboration and teamwork abilities, including cross-functional communication with stakeholders.

Preferred Skills

• Proven experience with detection and segmentation algorithms for radar image data.

• Exposure to research collaboration with academic institutions (e.g., NSERC, MITACS) and industrial R&D partners.

• Familiarity with deploying trustworthy and certifiable AI models in critical applications.

• Background in developing AI models under resource constraints (e.g., frugal, few-shot, zero-shot learning).

• Patent contributions or innovation disclosures are a plus.

Key Responsibilities

• Conduct advanced research in AI and computer vision, focusing on image/video processing, deep learning, and innovative algorithm development.

• Design and implement high-performing models for real-world tasks such as object detection, segmentation, and tracking.

• Lead exploration of frugal learning approaches to maximize performance from minimal training data.

• Validate robustness and reliability of machine learning models under practical deployment conditions.

• Transition research into functional prototypes and production-ready solutions in collaboration with engineering teams.

• Contribute to strategic research roadmaps by translating stakeholder requirements into innovative research objectives.

• Publish and present research findings at top-tier conferences and contribute to patents and internal knowledge bases.

• Serve as a subject matter expert in cross-disciplinary project teams, providing technical guidance and mentorship.

If you are a forward-thinking researcher ready to take on complex challenges in a dynamic, innovation-driven environment, this is your opportunity to make a meaningful impact in the AI space.

Join the Team!

Are you ready to take on exciting challenges in a dynamic and fast-paced environment? At NanoXplore, we offer an opportunity to be part of a rapidly growing company that is at the forefront of creating sustainable products, pushing the boundaries of innovation across multiple industries.

We believe in fostering creativity and encouraging fresh ideas—whether big or small—because innovation is at the heart of everything we do. Joining our team means you'll have the chance to contribute to groundbreaking solutions, collaborate with talented professionals, and make a real impact on a global scale.

If you're looking to grow, innovate, and make a difference, NanoXplore is the place for you!

Summary Of The Role

Lead and support research and development activities focused on thermoplastics and polymer composites, while also providing technical expertise to the Sales Team. The role bridges internal R&D efforts with customer-facing initiatives by managing customer projects, supporting business development, and ensuring effective collaboration between labs, external partners, and customers.

Key Responsabilities

• Lead technical activities and manage the day-to-day operations of assigned R&D projects;
• Plan and execute tasks to ensure timely progress toward the goals of R&D and Sales-related projects and programs;
• Provide technical support to the Sales and Marketing teams;
• Participate in customer meetings to offer technical support and develop project proposals aligned with customer needs;
• Contribute to internal and external meetings, seminars, and discussions related to R&D and Sales initiatives;
• Prepare and deliver progress reports on R&D activities; support the R&D Manager in drafting program updates and documentation;
• Maintain up-to-date knowledge and technical expertise in relevant fields;
• Develop design of experiments for new R&D projects in collaboration with customers, partners, and collaborators, subject to written approval from R&D managers;
• Ensure compliance with company policies, methodologies, and project standards;
• Identify and communicate potential risks or challenges related to R&D projects to R&D managers.

Qualifications

• Master or PhD in materials/polymers engineering or chemical/mechanical engineering or related fields;
• Strong background in plastics, polymer resins, and advanced materials, with the ability to leverage this expertise to identify business opportunities, support sales, and solve industrial technical challenges;
• Solid understanding of polymer fundamentals (both thermosets and thermoplastics) and related performance requirements, as well as familiarity with polymer processing equipment;
• Practical knowledge of the application of polymer fillers, stabilizers, and additives;
• Proven experimental expertise in understanding and applying polymer structure–property relationships.

Skills & Attitude

• Strong organizational skills with the ability to manage multiple tasks and priorities effectively;
• Proven ability to define problems, collect and analyze data, and draw valid conclusions;
• Excellent time management and clear, effective communication skills;
• Reliable and dependable;
• Creative in developing technical solutions;
• Hardworking and committed;
• Adaptable to shifting priorities and organizational changes;
• Maintains a positive, proactive attitude;
• Strong interpersonal skills;
• Team-oriented, able to contribute effectively to fast-paced projects.

At NanoXplore, we value our employees and offer a comprehensive benefits package to support your well-being:

• RRSP/DPSP program;
• Group insurance program including medical and dental coverage;
• Telemedicine program for you and your immediate family;
• Employee and family assistance program;
• Free on-site gym;
• Regularly organized social events (potluck, BBQ and more).

___

Rejoignez l'équipe!

Êtes-vous prêt(e) à relever des défis passionnants dans un environnement dynamique et stimulant ? Chez NanoXplore, nous vous offrons l'opportunité de rejoindre une entreprise en pleine croissance, à la pointe de l'innovation, qui crée des produits durables et repousse les limites dans divers secteurs industriels.

L'innovation est au cœur de nos valeurs, et nous encourageons les idées nouvelles, qu'elles soient grandes ou petites. En rejoignant notre équipe, vous aurez l'occasion de contribuer à des solutions révolutionnaires, de collaborer avec des professionnels talentueux et d'avoir un impact réel à l'échelle mondiale.

Si vous êtes prêt(e) à grandir, à innover et à faire une différence, NanoXplore est l'endroit idéal pour vous !

Sommaire du rôle

Diriger et soutenir les activités de recherche et développement axées sur les thermoplastiques et les composites polymères, tout en fournissant une expertise technique à l'équipe de vente. Le rôle fait le lien entre les efforts internes de R&D et les initiatives orientées vers les clients en gérant les projets clients, en soutenant le développement commercial et en assurant une collaboration efficace entre les laboratoires, les partenaires externes et les clients.

Responsabilités clés

• Diriger les activités techniques et gérer les opérations quotidiennes des projets de R&D assignés;
• Planifier et exécuter les tâches pour assurer une progression rapide et conforme aux objectifs des projets et programmes liés à la R&D et aux ventes;
• Fournir un support technique aux équipes de vente et de marketing;
• Participer aux réunions avec les clients pour offrir un support technique et développer des propositions de projet en adéquation avec les besoins des clients;
• Contribuer aux réunions internes et externes, séminaires et discussions liés aux initiatives de R&D et de ventes;
• Préparer et livrer des rapports d'avancement sur les activités de R&D; soutenir la Directrice de la R&D dans la rédaction des mises à jour et de la documentation des programmes;
• Maintenir des connaissances et une expertise technique à jour dans les domaines pertinents;
• Développer des plans d'expériences pour les nouveaux projets de R&D en collaboration avec les clients, partenaires et collaborateurs, sous réserve de l'approbation écrite des responsables de la R&D;
• Veiller au respect des politiques, méthodologies et normes de projet de l’entreprise;
• Identifier et communiquer les risques ou défis potentiels liés aux projets de R&D aux responsables de la R&D.

Qualifications

• Maîtrise ou doctorat en ingénierie des matériaux/polymères ou en ingénierie chimique/mécanique ou dans des domaines connexes;
• Une expérience démontrée dans le domaine des plastiques, des résines polymères et des matériaux avancés ainsi que la capacité d'utiliser cette expertise pour identifier les opportunités commerciales, soutenir les ventes et résoudre les problèmes techniques industriels;
• Une compréhension approfondie des fondamentaux des polymères (thermodurcissables et thermoplastiques) et des exigences de performance ainsi qu’une familiarité avec les équipements de traitement des polymères;
• Compréhension pratique de l'application des charges, des stabilisants et des additifs des polymères;
• Expertise avérée dans la compréhension et l’application des relations structure-propriété des polymères (expérimentale).

Habiletés

• Excellent sens de l'organisation, y compris la capacité de gérer efficacement plusieurs tâches et priorités;
• Capable de définir des problèmes, de collecter des données, d'établir des faits et de tirer des conclusions valables;
• Excellentes compétences en matière de gestion du temps;
• Fiabilité;
• Créatif dans le développement de solutions techniques;
• Travaillant et engagé;
• Adaptabilité face aux priorités changeantes;
• Attitude positive et proactive;
• Excellentes compétences interpersonnelles;
• Capacité à travailler en équipe sur des projets au rythme rapide.

Chez NanoXplore, nous valorisons nos Employés et offrons un ensemble complet d'avantages pour soutenir votre bien-être:

• Programme REER/RPDB;
• Programme d'assurance collective comprenant une couverture médicale et dentaire ;
• Programme de télémédecine accessible pour vous et votre famille immédiate;
• Programme d'aide aux employés et aux familles;
• Salle de sport gratuite sur place;
• Événements sociaux organisés régulièrement (potluck, barbecue et autres).