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361 Research Associate jobs in Canada

Research Assistant or Research Associate

Vanier, Ontario Akausivik Inuit Family Health Team

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Job Description

Salary:

The Akausivik Inuit Family Health Team (AIFHT) is a not-for-profit health clinic dedicated to delivering culturally competent, high-quality care to the Inuit community. AIFHT works collaboratively with federal, provincial, and local health authorities to ensure we are responsive and rooted in a model of excellence in primary care.

AIFHT is currently looking for a Research Assistant/Associate to join our team in a one-year term position (with the potential for extension). The Research Assistant/Associate will support health research activities led by our organization. This includes gathering data, preparing, and distributing surveys, supporting stakeholder engagement, and assisting in other research-related tasks. This role will be based in a medical setting and will involve both administrative and field-based research responsibilities.

The position reports to the Executive Director and receives day-to-day guidance and support from the Research Project Manager.

KEY RESPONSIBILITIES:

  • Assist with the collection and management of research data.
  • Conduct interviews with survey or study participants.
  • Participate in consultations with stakeholders (including Inuit participants and organizations at local, regional, and national levels).
  • Prepare meeting materials, schedule sessions, and take meeting minutes as needed.
  • Maintain accurate and confidential records, including research and participant files.
  • Assist in drafting reports, summaries, and research documentation.
  • Support overall research team coordination and communication.
  • Perform other related duties as assigned.

QUALIFICATIONS & EXPERIENCE:

  • Post-secondary education in Health Research, Social Sciences, Office/Project Administration, or equivalent combination of training and experience.
  • 1 - 2 years of experience in research or administrative roles (related experience is considered an asset).
  • Strong written and verbal communication skills.
  • Proficiency with Microsoft Office, internet-based research tools, and basic data management.
  • Knowledge of Inuit health-related challenges in a cultural context.
  • Highly organized and able to manage multiple tasks in a dynamic, client-facing environment.
  • Fluency in Inuktitut is a strong asset.

WORKING CONDITIONS:

  • May be required to work occasional evening or weekend shifts depending on project needs.
  • This is a full-time, term position with potential for renewal based on funding and performance.

APPLICATION DETAILS:

Preference in hiring will be given to qualified candidates with Inuit Ancestry as directly relevant to the skills and knowledge for this position. The successful candidate will be required to submit a Criminal Record Check, with Vulnerable Sector Screening.

Only those selected for an interview will be contacted. We thank all applicants for their interest.


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Senior Research Associate

Toronto, Ontario $90000 - $120000 Y Canada China Business Council | Conseil d'affaires Canada-Chine

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The
Canada China Business Council (CCBC)
is seeking a dedicated and skilled full-time Senior Research Associate to join its corporate head office in Toronto for a 12-month contract, with the possibility of extension and transition into a permanent role. This position is based in a fast-paced, dynamic work environment that requires the ability to manage multiple deadlines, competing priorities, and quick turnarounds.

The Senior Research Associate will report directly to the Executive Director and Chief Operating Officer and work closely with CCBC's Communications Manager and regional teams. This role bridges policy-relevant research and strategic communications. You will support the Council's thought leadership work by conducting original research and its public positioning by producing high-impact written materials, conducting background research, preparing knowledge- and research-based content for presentations, and contributing to executive-level communications. This is a research-, writing-, and insight-driven role ideal for an experienced policy-savvy researcher and communicator who can synthesize complex trade, policy, and business issues into compelling, audience-friendly knowledge products and content.

Key Responsibilities

Includes but not limited to:

·  Conduct original research and monitor developments related to:

o Canada–China business and economic relations

o Trade policy, bilateral and multilateral agreements, and foreign investment trends

o Sector-specific dynamics impacting CCBC members (e.g., energy, natural resources, agriculture, education, financial services, life sciences)

o Canadian and Chinese government priorities, regulations, and policy documents relevant to CCBC members

o Canada's trade strategy and Asia Pacific policy as it relates to China

·   Draft, edit, and fact-check high-quality written materials, including:

o Thought leadership pieces (policy briefs, op-eds, blogs, commentary)

o Executive speeches, talking points, and presentations

o Reports, briefings, backgrounders, and memos

o Web and social media content, in collaboration with the Communications Manager

·   Analyze Canada-China trade and investment data to support research outputs, briefings, and sector-specific insights for CCBC members and stakeholders.

·   Support CCBC's media and public relations efforts by preparing briefing notes, Q&A docs, and reactive messaging.

·   Assist in preparing internal and external reports.

·   Provide research support for CCBC's signature events, such as the Annual General Meeting and policy forums.

·   Plan and organize educational events, webinars and learning programs for members, focused on key policy, trade, and sectoral developments.

Qualifications & Experience


• 3-5 years of relevant experience in policy research, strategic communications, public affairs, or a related field, with demonstrated expertise in Canada–China or broader Canada–Asia trade, economic, and foreign policy issues gained through academic, professional, or policy-focused work.


• Strong analytical and research skills, with the ability to synthesize complex information quickly and clearly.


• Experience working with trade, investment, or economic data—such as Statistics Canada, UN Comtrade, or Chinese government sources—with the ability to interpret and present key trends clearly.


• Educational background in international relations, economics, public policy, or business, with demonstrated focus on Asia-Pacific or China. A relevant research-based graduate degree is an asset.


• Proven experience writing and editing for executive-level audiences in a business, policy, or media environment.


• Exceptional English writing and editing skills are essential; proficiency in French is a strong asset but not required.


• Comfortable working in a fast-paced environment, managing multiple deadlines and priorities with minimal supervision.

Work Environment & Location

This role follows a hybrid work model. Candidates based in Toronto are preferred given the location of CCBC's headquarters and core team activities; however, strong candidates based in Ottawa or other CCBC chapter centres in Canada (Montreal, Vancouver, Calgary, Halifax) are also encouraged to apply.

To Apply

Interested candidates should submit a resume, a one-page cover letter outlining their interest in the position and relevant experience, and a sample research paper—preferably related to the Council's work (e.g., Canada–China economic relations, the Chinese economy, or related topics)—to by end of day on
September 30, 2025
. Please reference "Senior Research Associate" in the subject line.

We thank all applicants for their interest; however, only those selected for an interview will be contacted.
No phone calls, please.

Eligibility:
You must be legally eligible to work for a Canadian company and provide a clear Criminal Background Check in order to be considered for this position.

DISCLAIMER:
The Canada China Business Council is an equal opportunity employer and is committed to providing employment accommodation in accordance with the 
Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act
. If contacted for an employment opportunity or testing, please advise Human Resources if you require accommodation.

About the Canada China Business Council (CCBC)

Founded in 1978, CCBC has been the leading voice of Canadian businesses in China for over 45 years, providing the knowledge and connections needed to succeed in China and Canada. In addition to its focused and practical services, CCBC is the voice of the Canadian business community on issues affecting Canada-China business, trade, and investment. Along with its corporate head office in Toronto, CCBC has chapters in Ontario, Quebec, the Atlantic region, British Columbia, the Prairies, Beijing, and Shanghai. CCBC's network of staff offers programs and services in both Canada and China, and introduces members to opportunities in China's emerging markets. CCBC also operates a Chamber of Commerce in Beijing, offering a range of events and broad networking opportunities at the local level.

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Equity Research Associate

$60000 - $80000 Y Canaccord Genuity Group Inc.

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Who we are:
Canaccord Genuity (CG) is a leading independent full-service financial services firm, with operations in two principal segments of the securities industry: wealth management and capital markets. CG is driven by an unwavering commitment to building lasting client relationships – we achieve this by generating value for our individual, institutional, and corporate clients through comprehensive investment solutions, brokerage, and investment banking services. We are the leading independent wealth management firm in Canada, and the leading mid-market provider of investment banking advisory, equity research, sales and trading services for corporations and institutions.

We pride ourselves on understanding our clients' needs and finding innovative, tailored solutions. Our entrepreneurial and friendly team will challenge you to learn and grow every day. We value great work and collaboration and strive to eliminate bureaucratic thinking. We're looking for talented people who thrive in a fast-paced environment and want to have an impact with innovative ideas and best practices.

Our Canadian operations are currently looking for a motivated team player to join us as a Research Associate with our Capital Goods team in Toronto or Montreal.

Responsibilities:

  • Provide research support to the Research Analyst;
  • Develop and maintain complex financial models;
  • Conduct company, industry and macro-economic research;
  • Coordinate, generate and maintain presentations and databases;
  • Assist in the writing of company and sector reports;
  • Assist with coordinating quarterly reporting initiatives;
  • Support and answer institutional client queries;
  • Coordinate special projects, presentations and initiatives as assigned.

Skills & Qualifications:

  • A post-secondary degree in Finance or Business, with at least two years of related experience;
  • CFA / CPA designation or path toward completion an asset;
  • Demonstrated interest in public companies and markets;
  • Direct experience with, and a solid understanding of, financial modeling & valuation analysis;
  • Advanced MS Office skills (Excel, Word, PowerPoint);
  • Bloomberg / FactSet proficiency;
  • Excellent written and verbal communication skills;
  • Excellent attention to detail;
  • Ability to create high-quality deliverables while managing multiple priorities in a fast-paced, dynamic work environment;
  • Solid work ethic with a demonstrated ability to work independently and as part of a team.
  • Willingness and flexibility to work long hours under deadline pressure and to show initiative.

___

Associé, Recherche sur les actions – Biens d'équipement
Toronto (Ontario) ou Montréal (Québec)
Qui nous sommes :
Canaccord Genuity (CG) est une société de services financiers indépendante de premier plan, offrant une gamme complète de services et exerçant ses activités dans deux principaux secteurs de l'industrie des valeurs mobilières : la gestion de patrimoine et les marchés des capitaux. CG est animée par un engagement inébranlable à bâtir des relations durables avec ses clients – nous y parvenons en générant de la valeur pour nos clients particuliers, institutionnels et entreprises grâce à des solutions de placement complètes, des services de courtage et des services bancaires d'investissement. Nous sommes la plus importante société indépendante de gestion de patrimoine au Canada, et le principal fournisseur de services-conseils en financement d'entreprises, de recherche sur les actions, et de vente et de négociation pour les sociétés et les institutions du marché intermédiaire.

Nous sommes fiers de comprendre les besoins de nos clients et de trouver des solutions novatrices et adaptées. Notre équipe entrepreneuriale et amicale vous mettra au défi d'apprendre et de vous perfectionner chaque jour. Nous valorisons l'excellent travail et la collaboration, et nous nous efforçons d'éliminer la pensée bureaucratique. Nous recherchons des personnes talentueuses qui s'épanouissent dans un environnement au rythme rapide et qui souhaitent avoir un impact grâce à des idées novatrices et aux meilleures pratiques.

Nos activités canadiennes sont actuellement à la recherche d'un joueur d'équipe motivé pour se joindre à nous à titre d'associé de recherche au sein de notre équipe des biens d'équipement à Toronto ou à Montréal.

Responsabilités :

  • Fournir un soutien à la recherche à l'analyste de recherche;
  • Élaborer et tenir des modèles financiers complexes;
  • Mener des recherches sur l'entreprise, le secteur et la macroéconomie;
  • Coordonner, générer et maintenir les présentations et les bases de données;
  • Aider à la rédaction de rapports sur l'entreprise et le secteur;
  • Aider à coordonner les initiatives de rapports trimestriels;
  • Soutenir les clients institutionnels et répondre à leurs questions;
  • Coordonner les projets spéciaux, les présentations et les initiatives, selon les directives.

Compétences et qualifications :

  • Un diplôme d'études postsecondaires en finance ou en administration des affaires, avec au moins deux ans d'expérience connexe;
  • La désignation CFA/CPA ou le cheminement vers son obtention est un atout;
  • Intérêt démontré pour les sociétés ouvertes et les marchés;
  • Expérience directe et compréhension approfondie de la modélisation financière et de l'analyse d'évaluation;
  • Maîtrise avancée de MS Office (Excel, Word, PowerPoint);
  • Maîtrise de Bloomberg/FactSet;
  • Excellentes aptitudes à la communication écrite et verbale;
  • Excellente attention aux détails;
  • Capacité à créer des livrables de haute qualité tout en gérant de multiples priorités dans un environnement de travail dynamique et en évolution rapide;
  • Solide éthique de travail avec une capacité démontrée à travailler de façon autonome et en équipe.
  • Volonté et souplesse pour travailler de longues heures sous la pression des délais et pour faire preuve d'initiative.

All applications will be held in strict confidence.

In order to be considered for employment, candidates selected for interviews will be required to show proof of citizenship, permanent residence or eligibility to work in Canada with no restrictions.

Protecting your online safety:
Canaccord Genuity and its affiliates do not use text messages for recruitment purposes. If you have received a text message claiming to be from CG or an authorized representative regarding job recruitment, please treat as fraudulent and do not respond.

We wish to thank all candidates for their interest but only those applicants selected for an interview will be contacted. No phone calls please. Thank you for your understanding.

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Research Associate, Preclinical

Vancouver, British Columbia Acuitas

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Job Description

Salary: $80,000-$00,000

Acuitas Therapeutics is a private biotechnology company located at 6190 Agronomy Rd #402, Vancouver,British Columbia, Canada. We are the premier global provider of LNP delivery systems for nucleic acid therapeutics. Acuitas is partnered with multiple international, biotechnology and pharmaceutical partners who are focused on bringing new vaccines and drugs into clinical development and to the marketplace.


At Acuitas, we believe in combining excellent science with an enviable work culture. The advanced LNP technologies we provide for our partners are made possible by our employees who apply their passion, curiosity, and knowledge every step of the way. At Acuitas, you will have the opportunity to work as part of a close-knit team of exceptional scientists, who support the production of revolutionary technology that impacts the health and wellness of society. By living our values, including honesty, integrity, innovation and openness, we have fostered a supportive work environment where our employees feel empowered, challenged, recognized and rewarded. If you would like to work for a company that is at the top of the field, Acuitas is the company for you!


All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or any other status protected by applicable law.



Job Title: Research Associate, Preclinical


YOU: A committed professional with experience in preclinical research looking to develop further in an innovative, fast paced biotech environment.

US: Leading innovators in the lipid nanoparticle (LNP) field, looking for a talented individual to join our collaborative, passionate, and diverse results focused team.

ROLE SUMMARY: Acuitas Therapeutics is seeking a permanent, full-time Research Associate with a strong background in immunology and immunological methods to work in the Preclinical team, reporting to the Senior Research Scientist, Preclinical. The role holder will be responsible for executing and supporting studies assessing the pharmacology, immunology, mechanism of action, distribution and safety profile of our LNP, executing analyses and data interpretation, and presenting results to the team and company.

Working with the Preclinical team, the responsibilities would include:

  1. Executing and supporting studies to evaluate LNP activity, distribution, mechanisms of action, immune profiles and safety.
  2. Mastering established methods and developing new methods to support preclinical objectives, including ELISA, MSD, luciferase assays, qPCR, SDS-PAGE, DNA/RNA isolation and protein quantification.
  3. Cell culture and cell-based assays (including ELIspot), cell isolation, and processing tissues and fluids for downstream analysis.
  4. Hands-on experience in multi-colour flow cytometry, intracellular cytokine staining and gating strategies.
  5. General laboratory support including preparation of reagents and solutions, laboratory organization, maintaining sample and reagent inventory, and shipping of materials.
  6. Up to date Biosafety/Biosecurity (Containment Level 2+) and WHMIS certification will be required.
  7. Maintain familiarity with relevant scientific knowledge and advancements in LNP technology.
  8. May be required to train more junior staff and co-op students.



QUALIFICATIONS AND SKILLS:

  • BSc with 2-10 years experience or an MSc with up to 7 years experience; some industry experience preferred.
  • Hands-on experience conducting experiments with LNP in vitro and ex vivo; knowledge of LNP formulation processes, LNP characteristics, in vivo biodistribution, pharmacodynamics and pharmacokinetics
  • Strong background in innate and adaptive immunology. Knowledge specific to LNP preferred.
  • Strong understanding of cell biology and human physiology with a focus on liver structure and function as well as other fenestrated organs.
  • Background in vaccine development and experience conducting/analyzing associated assays (ELISA, EliSpot, HAI)
  • Hands-on experience in tissue isolation, single cell preparation, cell culture, cell-based assays and cell differentiation.
  • Extensive experience in multiplex immune-based assays. Specifically Meso Scale Diagnostics and multichannel flow cytometry including the development of gating strategies.
  • Confident and proven safety when working in Biosafety Level 2+ environments.
  • Excellent writing and presentation skills. Accurate and appropriate data analysis and use of statistics.
  • Familiar with Spotfire and Big Omics or similar visualization platforms. Fluent working with Graph Pad and Microsoft Office. Adept utilizing Flo Jo or similar.
  • Responsible and reliable record keeping, organization and assisting in lab management as needed.
  • Very strong communicator in English language


Benefits
Health benefits
Dental plan
Disability benefits
Health care plan
Paramedical services coverage
Vision care benefits


Financial benefits
Bonus
Group insurance benefits
Life insurance
Registered Retirement Savings Plan (RRSP)
Long term benefits
Maternity and parental benefits
Other benefits
Learning/training paid by employer
On-site amenities
Paid time off (volunteering or personal days)


Compensation

80,000- 100,000 per annum


Contact:



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Senior Clinical Research Associate

ICON Clinical Research

Posted 10 days ago

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Clinical Research Associate, Toronto, Canada, Oncology Required
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 CRA you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
En tant qu'ARC (Associé(e) de recherche clinique), vous rejoindrez la plus grande et la plus complète organisation de recherche clinique au monde, propulsée par l'intelligence en santé.
**What You Will Be Doing:**
+ Contribute to the identification of new sites for clinical trials
+ Assume ambassadorial role to facilitate communication between sites and sponsor CPO to increase value proposition to investigators.
+ Facilitate the preparation and collection of site and country level documents during all phases of the trial. Supports the Clinical Study Manager in the oversight of Country and Site Trial Master Files (TMF). During all phases of the trial ensure archiving per relevant SOP.
+ Execute site initiation and training, generate initiation visit report.
+ Implement complete site management including monitoring visits, regulatory assessment, drug supply management, etc. to ensure compliance with protocol, GCP, global and local regulations, global and local processes.
+ Identify problems at sites; resolve issues and escalate as appropriate.
+ Complete preparation and generation of visit monitoring reports as per relevant SOP.
+ Review and manage data at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.
+ Implement site close-out activities and generate site close-out report.
+ Provide feedback on site performance for future trial site feasibility/selection
+ Improve skills by timely completion performance of assigned global and local training.
+ **Responsabilités:**
+ Contribuer à l'identification de nouveaux centres pour des études cliniques
+ Assumer un rôle d'ambassadeur pour faciliter les communications entre les centres d'étude et le Directeur de l'expérience patient du promoteur, afin de rehausser la proposition de valeur aux chercheurs.
+ Faciliter la préparation et la collecte des documents aux centres d'étude et à l'échelle du pays pendant toutes les phases d'étude. Soutenir le travail du gestionnaire de l'étude clinique pour la surveillance des fichiers maîtres de l'étude (FME) aux centres d'étude et à l'échelle du pays. Pendant toutes les phases d'étude, s'assurer que l'archivage est conforme aux procédures d'exploitation normalisées.
+ Effectuer l'initiation des centres d'étude et la formation du personnel, rédiger le rapport de la visite d'initiation.
+ Mettre en place la structure complète de gestion des centres d'étude, entre autres, les visites de surveillance, les évaluations réglementaires, la gestion de l'approvisionnement en médicaments, pour assurer la conformité au protocole, aux BPC, aux réglementations mondiales et locales, et aux processus mondiaux et locaux.
+ Identifier les problèmes aux centres d'étude; résoudre les problèmes et les communiquer à un palier supérieur de la direction, le cas échéant.
+ Effectuer la rédaction complète et la distribution des rapports sur les visites de surveillance, conformément aux procédures d'exploitation normalisées pertinentes.
+ Examiner et gérer continuellement les données recueillies aux centres d'étude, afin de résoudre rapidement les problèmes techniques et de contenu pour atteindre les cibles de verrouillage de la base de données en temps opportun.
+ Mettre en œuvre les activités de clôture des centres d'étude et rédiger le rapport de clôture des centres d'étude.
+ Fournir des commentaires sur les performances des centres d'étude afin d'évaluer leur candidature pour de futures études cliniques.
**Your Profile:**
+ Bachelor's Degree or higher in life sciences or equivalent
+ Minimum 2 years' clinical site monitoring experience from CRO or Pharmaceutical company
+ Comprehensive knowledge and understanding of ICH-GCP
+ Able and willing to travel up to 60% regionally (sites in Quebec City and Montreal)
+ Able and willing to work on several protocols/therapy areas
+ Experience in phase I-IV trials
+ Working knowledge of Electronic Data Capture (preferred)
+ Experience/working knowledge of the oncology disease area (preferred but not required)
+ Experience of Centralized/Risk Based/Targeted monitoring (preferred)
+ Experience of working within a metric based environment (preferred)
+ Excellent attention to detail
+ Highly developed time management and organizational skills
+ Focused on meeting study deliverables/targets
+ Flexible and willing to adapt to changing priorities/timelines
+ Experience in oncology is required
+ Blingual English/French Required
**Compétences**
+ Baccalauréat ou diplôme supérieur en sciences de la vie ou un équivalent
+ Minimum de 2 à 4 ans d'expérience en surveillance de centres d'étude pour une entreprise de recherche contractuelle ou une société pharmaceutique
+ Des connaissances et une compréhension approfondies des bonnes pratiques cliniques élaborées par la Conférence internationale sur l'harmonisation (BPC-CIH)
+ Bilinguisme français/anglais (maîtrise verbale et écrite) exigé
+ Disposé(e) et apte à voyager jusqu'à 60 % du temps à l'échelle régionale (centres d'étude à Québec et à Montréal)
+ Disposé(e) et apte à travailler sur plusieurs protocoles/domaines thérapeutiques
+ Expérience dans les études cliniques de phase I à IV
+ Connaissance pratique de la saisie électronique des données (préférable)
+ Expérience/connaissance pratique dans le domaine des maladies oncologiques (préférable, mais non requise)
+ Expérience dans la surveillance centralisée/axée sur les risques/ciblée (préférable)
+ Expérience de travail dans un environnement métrique (préférable)
+ Souci du détail
+ Compétences organisationnelles et de gestion du temps de haut niveau
+ Déterminé(e) à fournir les livrables et atteindre les objectifs des études
+ Flexible et disposé(e) à s'adapter aux changements dans les priorités/échéanciers
**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 maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At 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, 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 or submit a request here ( 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.
Are you a current ICON Employee? Please click here ( to apply
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Research Associate - Infrastructure Insights

New Brunswick, New Brunswick Bentley Systems

Posted 15 days ago

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**Research Associate**
**Infrastructure Insights**
**Location:** Canada
**Work mode:** Home Based - Hybrid
**Position Summary:**
The **Research Associate - Infrastructure Insights** plays a key role in advancing Bentley's mission to inform and inspire positive change across the global infrastructure ecosystem. Sitting within the Infrastructure Policy & Advocacy (IPA) initiative, this role leads industry-insight monitoring and reporting for Bentley's leadership team.
You will design and manage a scalable research process to identify and track emerging trends in infrastructure markets, develop productive relationships with industry membership bodies, and deliver quarterly data-driven reports that help shape Bentley's strategic direction. This position offers the opportunity to collaborate across teams and ensure research outputs are accessible, inclusive, and aligned with Bentley's commitment to sustainability, innovation, and equity.
_Note: This role is internally titled_ **_Infrastructure Insights Lead_** _, reflecting its strategic scope and leadership responsibilities within the IPA initiative._
**Responsibilities:**
+ Lead the IPA's industry-insight monitoring and reporting function, developing a scalable process for market research and reporting that can grow across regions and business functions.
+ Conduct desk-based research and engage stakeholders - including industry associations and relevant bodies - to analyze:
+ Global developments across infrastructure sectors (transport, water, energy, etc.)
+ Infrastructure policy and investment trends in Bentley's key markets
+ Innovative funding, finance, and delivery models
+ Digital transformation trends in infrastructure
+ Synthesize research findings into quarterly insight reports, briefing notes, market scans, and landscape analyses to support Bentley's programs and partnerships.
+ Develop and maintain a knowledge base of relevant data sources, stakeholders, and industry initiatives, ensuring insights are accurate, timely, and broadly accessible to internal stakeholders.
+ Collaborate with cross-functional teams to support inclusive decision-making and knowledge sharing.
**Qualifications:**
+ Bachelor's degree in public policy, management, engineering, urban planning, economics, or a related field; Master's degree preferred but not required.
+ 5+ years of experience in research, consulting, or policy analysis, ideally within infrastructure or the built environment.
+ Strong analytical and critical thinking skills, with the ability to synthesize complex information into clear, actionable insights.
+ Excellent written and verbal communication skills in English (near-native fluency required); additional languages are a plus.
+ Self-starter with strong organizational skills, attention to detail, and a collaborative mindset.
+ Familiarity with infrastructure markets, public policy, and international business - or the ability to quickly learn and adapt.
+ Commitment to Bentley's values, including sustainability, innovation, and fostering an inclusive workplace.
+ We encourage candidates from diverse backgrounds to apply, even if you do not meet 100% of the listed qualifications.
**What We Offer:**
+ A great Team and culture - please see our colleague video .
+ An exciting career as an integral part of a world-leading software company providing solutions for architecture, engineering, and construction - watch this short documentary about how we got our start.
+ An attractive salary and benefits package.
+ A commitment to inclusion, belonging and colleague wellbeing through global initiatives and resource groups.
+ A company committed to making a real difference by advancing the world's infrastructure for better quality of life, where your contributions help build a more sustainable, connected, and resilient world. Discover our latest user success stories for an insight into our global impact.
**LI-BC #LI-Hybrid #LI-Remote**
 **About Bentley Systems**
Around the world, infrastructure professionals rely on software from Bentley Systems to help them design, build, and operate better and more resilient infrastructure for transportation, water, energy, cities, and more. Founded in 1984 by engineers for engineers, Bentley is the partner of choice for engineering firms and owner-operators worldwide, with software that spans engineering disciplines, industry sectors, and all phases of the infrastructure lifecycle. Through our digital twin solutions, we help infrastructure professionals unlock the value of their data to transform project delivery and asset performance. Opportunity Employer:**
Bentley is proud to be an equal opportunity employer and considers for employment all qualified applicants without regard to race, color, gender/gender identity, sexual orientation, disability, marital status, religion/belief, national origin, caste, age, or any other characteristic protected by local law or unrelated to job qualifications.
Equal Opportunity Employer/Minorities/Females/Veterans/Disabled
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Research Associate I, Translational Biology

Vancouver, British Columbia $67800 - $83800 Y Borealis Biosciences, Inc.

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Job Description

Company:

Chronic kidney disease (CKD) is a serious and growing global health challenge, affecting approximately 1 in 7 people worldwide. In the absence of effective treatments, patients may progress to kidney failure, requiring dialysis or transplantation—placing a significant burden on patients, families, and healthcare systems. While recent advances have benefited certain subsets of kidney disease patients, many common forms of CKD still lack effective therapeutic options.

Borealis was founded on the belief that the convergence of scientific and translational breakthroughs can unlock the potential of RNA therapeutics to address some of the most rare and underserved kidney diseases—and beyond. Borealis builds on the success of Chinook Therapeutics, a kidney disease company with a research site in Vancouver that was acquired by Novartis in 2023 for $3.5 billion. The Borealis team has strong leadership and academic advisors with deep experience and expertise in both kidney disease and RNA therapeutics. Headquartered in Vancouver, BC, Borealis operates state-of-the-art wet labs equipped for molecular and cellular biology, in vivo pharmacology, chemistry, DMPK, bioinformatics, and analytical sciences.

We are a creative and innovative team that strives for excellence in all we do and have fun along the way. Our core focus is on helping patients and advancing science. For more information on Borealis, check out our sites &

We seek applicants from all backgrounds to ensure we get the best, most innovative talent on our team. We are building a diverse and inclusive workforce – come and be a part of our growth We strongly encourage candidates with less traditional backgrounds or those who may meet the qualifications in a different way to apply.

Position:

Borealis Biosciences is seeking an enthusiastic and collaborative Research Associate to join the Translational Biology & Pharmacology team at our laboratories situated in Vancouver, Canada. The successful candidate will spend the majority of their time performing, analyzing, and interpreting endpoint assays to support in vivo pharmacology workflows, generating critical data to inform go/no-go decisions in platform development and preclinical drug discovery activities. This position offers an exciting opportunity to work in an innovative and collaborative team with diverse scientific expertise and a focus on patients.

Responsibilities include:

  • Perform, analyze, and interpret in vitro and ex vivo endpoint assays to support the advancement of platform development goals and preclinical drug discovery programs.
  • Assist in the development of in vitro models to investigate target biology and underlying mechanisms.
  • Assist team members with in vivo study takedowns and sample collection for end point analyses.
  • Review research literature to inform experimental designs and contribute to overall project advancement.
  • Prepare clear and concise study protocols and technical reports and maintain accurate records in an electronic lab notebook (ELN).
  • Present experimental data and findings in team meetings and contribute to scientific discussions.
  • Support the maintenance of a clean, organized, and fully functional laboratory environment.
  • Foster and contribute to a collaborative, team-oriented, and positive company culture.

Location:

  • This is an on-site lab-based position located in Borealis Bio's Vancouver, BC headquarters. Most of your time will be spent conducting wet lab work.

Education, Experience, and Skills:

  • B.Sc. degree in a relevant scientific discipline and hands-on research experience— preferably in an industrial setting.
  • Direct experience in handling in vivo samples including plasma, serum, urine and tissues —exposure to in vivo necropsy and tissue collection techniques is a plus.
  • Extensive experience in cell culture, qPCR, and ELISA techniques.
  • Strong working knowledge of cellular biology, molecular biology, and biochemistry.
  • Proficient with Microsoft Office Suite and GraphPad Prism; experience with ELNs, such as Benchling or Dotmatics, is a plus.
  • Strong time management skills and ability to thrive in a fast-paced, cross-functional team environment.
  • Adaptability to shifting priorities and changing workloads.
  • A collaborative team player with a genuine passion for science and drug discovery.
  • Demonstrates a positive attitude, integrity, and high personal and ethical standards.

Compensation: The annual salary range is $7,800 - 83,800 and Borealis Bio provides competitive benefits including RRSP matching, extended medical, dental, vision and a Wellness Spending Account up to 1,800 per year. Actual base salary and title/level will be determined based on the qualifications of the successful candidate.

Borealis is an Equal Opportunity Employer, and we prohibit discrimination or harassment of any kind. We are committed to fostering an environment where ALL people are welcome and supported. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team – one that makes better decisions, drives innovation, and delivers better business results. Creativity and innovation flourish in an environment of openness, inclusion, and mutual respect.

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