13 Research And Development jobs in Ottawa
Senior DevOps Developer - Product Development Group
Posted 2 days ago
Job Viewed
Job Description
Job Description
Company Description
Canadian Bank Note Company (CBN) designs and develops industry leading solutions for the following domains: Border Security, Civil Identity, Driver Identification and Vehicle Information, Currency and Excise Control, and Lottery and Charitable Gaming. To learn more, visit
WHAT WE CAN OFFER YOU
- Compensation : We seek long term relationships with our employees and recognize and reward them with a competitive total compensation package that includes:
- An industry leading defined contribution pension plan with company matching contributions (up to 5%) and payment of service fees,
- Best-in-class health, medical and life insurance benefits;
- Access to virtual and telehealth services and apps; and
- Very progressive fertility, adoption and surrogacy benefits to support all definitions of family.
- Career : As a knowledge-based organization we will provide you with a wealth of learning opportunities and challenging work that will grow your knowledge, skills and abilities. At CBN, we encourage and empower our employees to chart their own career path, putting you in control of your future.
- Culture : Personal character is the foundation of our culture. CBN’s 7 Core Principles shape and guide our behaviours and underpin the sense of community you will experience at CBN. Equity, diversity and inclusivity are important to us as an organization, and we are committed to fostering and developing a work environment where every employee is treated with dignity and respect.
Internal Job Title: Senior DevOps Developer
Job Type: Permanent, Full-time
Job Location: 18 Auriga Drive, Ottawa, ON
Work Model: Hybrid (2-3 days/week on-site)
POSITION SUMMARY
As a Senior DevOps Developer in our Operations Production group, you will be responsible for driving DevOps practices to ensure efficient delivery of highly scalable and reliable modern cloud systems.
JOB DUTIES & RESPONSIBILITIES
DevOps Strategy and Implementation
- Design, develop and implement DevOps strategies and best practices to automate and streamline our software delivery processes.
- Select, implement, and maintain CI/CD pipeline tools that enable complete automation of build, test, and deployment.
Infrastructure Management
- Manage and optimize the Azure cloud, GitHub, and JFROG infrastructure and applications to ensure scalability, reliability, and cost-efficiency.
- Implement cloud security solutions to resolve system issues swiftly and effectively, ensuring the protection of internal information.
- Lead incident response and root cause analysis efforts to ensure timely resolution of production issues and minimize downtime.
Quality and Security
- Collaborate with cross-functional teams to improve input quality and content security through automation insights (i.e., SonarQube and JFROG Xray).
Continuous Improvement
- Proactive in continuous improvement that is data-driven through developed KPI reporting.
- Stay current with industry trends and emerging technologies in DevOps and cloud computing and evaluate their potential impact on our infrastructure and processes.
Miscellaneous
- Various other duties and responsibilities.
Knowledge and Experience
- Bachelor’s degree in Computer Science/Engineering (or similar) or equivalent combination of education and years of relevant work experience
- Knowledge of the following:
- Cloud computing platforms
- Microsoft/Azure DevOps
- CI/CD concepts, pipelines and tools
- Containerization and orchestration
- Networking, security and compliance requirements in cloud environments
- 3+ years of experience in a DevOps (or related) position
- 2+ years of experience with cloud infrastructure provisioning, configuration, and management
- 2+ years of experience in a software or Azure automation technical leadership position
- Github experience is an asset
Technical Skills
- Cloud: Azure, AWS
- Methodologies: DevOps, CI/CD
- Containerization/Orchestration: Docker, Kubernetes, Terraform
- Tools: Development pipeline (Jira/Bamboo, Jenkins, CircleCI, Gitlab CI/CD) and automation (Selenium, JUnit)
- Quality and Security : Static code analysis (SonarQube), vulnerability management (JFrog Xray) and secrets management (Hashicorp)
- Monitoring and Observability: Telemetry and visualization (Prometheus, Grafana) and application performance (New Relic, Datadog)
- Version Control : Git
Soft Skills and Characteristics
- Critical thinking skills
- Analysis, problem-solving
- Interpersonal skills
- Communication, teamwork and collaboration, leadership
- Growth mindset
Mandatory Requirements
- Fluency in English (reading, writing, verbal)
Security Clearance Requirements
- Ability to obtain and maintain Government of Canada Secret (Level II) personal security clearance.
Additional Information
As an Equal Opportunity Employer, CBN is committed to achieving a skilled workforce that reflects the diversity of the Canadian population. We welcome and encourage applications from individuals of all backgrounds, including but not limited to women, visible minorities, persons with disabilities, Indigenous peoples, and members of the 2SLGBTQ+ community.
CBN is committed to developing inclusive, barrier-free selection processes and work environments. If contacted regarding this competition, please advise the interview coordinator of any accommodation measures you may require.
Full Stack Developer - Product Development Group
Posted 2 days ago
Job Viewed
Job Description
Job Description
Company Description
Internal Job Title: Full Stack Software Developer
Job Type: Permanent, Full-Time
Job Location: 18 Auriga Drive, Ottawa ON
Work Model: Hybrid
Position Summary
As a Full Stack Developer in our Corporate Info Systems group, you will be responsible for designing, developing, and maintaining scalable applications. You will work closely with cross-functional teams including product owners, architects, and other developers to create seamless, efficient and high-quality solutions. Your expertise in both front-end and back-end technologies will be crucial in delivering high-quality, user-centric applications.
What We Can Offer You
- Compensation: We seek long term relationships with our employees and recognize and reward them with a competitive total compensation package that includes:
- An industry leading defined contribution pension plan with company matching contributions (up to 5%) and payment of service fees,
- Best-in-class health, medical and life insurance benefits;
- Access to virtual and telehealth services and apps; and
- Very progressive fertility, adoption and surrogacy benefits to support all definitions of family.
- Career: As a knowledge-based organization we will provide you with a wealth of learning opportunities and challenging work that will grow your knowledge, skills and abilities. At CBN, we encourage and empower our employees to chart their own career path, putting you in control of your future.
- Culture: Personal character is the foundation of our culture. CBN’s 7 Core Principles shape and guide our behaviours and underpin the sense of community you will experience at CBN. Equity, diversity and inclusivity are important to us as an organization, and we are committed to fostering and developing a work environment where every employee is treated with dignity and respect.
What You Will Do
- Application Development
- Design and develop applications that are robust, scalable and maintainable
- Develop and maintain both client-side and server-side components using modern technologies
- Ensure seamless integration between the front-end and back-end components
- Write clean, maintainable, and efficient code while adhering to industry best practices and CBN coding standards
- Use version control systems like Git to manage code changes and collaborate with other developers
- Document code and create technical documentation to ensure maintainability
- Troubleshooting & Optimization
- troubleshoot and debug complex issues across the stack
- Identify and resolve issues in both the front-end and back-end of the application
- Use debugging tools and techniques to diagnose and fix problems
- Conduct performance testing and profiling to identify and resolve bottlenecks
- Ensure the application is highly available and can recover quickly from failures
- Collaboration
- Collaborate with product owners, designers, and other developers to understand requirements and provide technical solutions
- Conduct code reviews and review code written by other developers to ensure it meets quality standards
- Provide constructive feedback and suggest improvements to enhance code quality
- Foster a culture of continuous improvement and knowledge sharing within the team
- Innovation
- Continuously learn about new technologies and industry trends
- Evaluate and incorporate new tools and technologies that can improve the development process
- Stay informed about best practices and emerging standards in web development
- Various Other Duties and Responsibilities
Knowledge and Experience
- Bachelor’s degree in computer science (or similar field) or equivalent combination of education and years of relevant work experience
- Knowledge of the following:
- Object oriented programming principles
- Three tier client-server architecture
- Automated testing
- Agile (SCRUM) development methodology
- 3+ years of software development experience
Technology
- Languages: Java
- Frameworks: Angular
- Databases: PostgreSQL/SQL Server
- Cloud: Azure dev ops
- Containerization: Docker
- Tools: ADO
Soft Skills and Characteristics
- Critical thinking skills
- Analysis, problem-solving
- Creative thinking skills
- Interpersonal skills
- Communication, teamwork and collaboration
- Organization and time management skills
- Growth mindset
- Self-directed
Mandatory Requirements
- Fluency in English
- Ability to work on-call on a rotational basis
- Ability to travel domestically and/or internationally approx. 5 weeks/year
Security Clearance Requirements
- Ability to obtain and maintain Government of Canada Secret (Level II) personal security clearance.
Additional Information
CBN designs and develops industry leading solutions for the following domains: Border Security, Civil Identity, Driver Identification and Vehicle Information, Currency and Excise Control, and Lottery and Charitable Gaming. To learn more, visit
As an Equal Opportunity Employer, Canadian Bank Note Company, Limited is committed to achieving a skilled workforce that reflects the diversity of the Canadian population. We encourage applications from women, visible minorities, people with disabilities and Aboriginal people. Canadian Bank Note Company Limited is committed to developing inclusive, barrier-free selection processes and work environments.
If contacted regarding this competition, please advise the interview coordinator of any accommodation measures you may require.
Hardware Product Development Manager - Defense / C5ISR
Posted 2 days ago
Job Viewed
Job Description
Hardware Product Development Manager - Onsite Position
We’re looking for highly motivated Product Development Manager (Hardware) to join our Ottawa, ON team, you will lead a dynamic group of Engineers responsible for the development of new products and the support of the existing product lines . You plan and oversee the product development related activities, ensuring objectives are accomplished to meet the business and customer objectives.
You will also work closely with other cross-functional team members in Engineering, New Product Introduction (NPI), Customer Support, Sales and Marketing. You coach, mentor, guide, and help nurture the development team to realize its full potential and adopt our culture of quality and customer satisfaction.
Location: Ottawa, ON
We Take Care of Our People
Paid Time Off I RRSP with Employer Match I Health and Wellness Benefits I Learning and Development Opportunities I Competitive Pay I Referral Program I Recognition I Employee Stock Purchase Plan I Inclusive & Supportive Culture *
Your Challenge
Supervise the work assignments of a highly knowledgeable and motivated project teams
- Be a hands-on leader who achieves success through modelling best practices and a service attitude
- Responsible for the career development, training and performance evaluations of staff allocated to the Engineering Team
- Facilitate and ensure individual and team roles and responsibilities are understood
- Establish effective practices to attract, develop, motivate and retain high caliber staff
- Help lead cross-functional problem-solving initiatives
- Review testing protocols for compliance with accepted standards and verifies testing results to ensure the desired functionality has been achieved
- Participate in bid/project activities such as defining architectures, developing technical proposals and providing detailed cost and schedule estimates
- Interact with customers regarding requirements and technical solutions
- Manage 3rd party relationships and coordination of work for cross site initiatives
- Pre- and Post-Sales support when needed by Product Marketing or Customer Support
What You Bring
- Bachelor's Degree in Electrical Engineering or Computer Science, Technologist Diploma or equivalent will be considered
- 8 years industry experience relating to electronics computing
- Prior experience in a managerial or leadership role is preferred
- Experience/familiarity in the following is an asset:
- Development of electronic assemblies for aerospace applications
- Design for manufacturing processes and techniques
- Design for rugged environments
- Open system standards such as VME, VPX, XMC and PMC
- Leading-edge Intel and NXP/Qualcomm processors (x86, PA, ARM)
- Leading-edge Broadcom Ethernet Switches
- High-end FPGA design
- Latest embedded industry technologies, such as Gen 3/4 PCI Express, 40GbE Ethernet, USB 3, DDR4 memory, etc.
- Working knowledge of PCB technologies including stack up definition, material selection, IPC etc.
- Experience with product configuration management
- DO-254 Safety Certification
- Demonstrated drive and ability to achieve goals in an innovative and fast paced environment
- Demonstrated ability to manage multiple tasks simultaneously and able to react to shifting priorities to meet business need
- Demonstrated creativity, foresight, and mature engineering judgment in anticipating and solving unprecedented engineering problems
- The candidate should be a results-oriented team player who leads by example, holds themselves accountable for performance, takes ownership of their responsibilities, and champions process improvement initiatives
- Self-confident leader capable of motivating and mentoring their staff
- Ability to estimate/schedule development projects
- Detailed knowledge of embedded computing systems architecture, hardware, software and related support requirements in the military/aerospace industry
- Team orientated and commitment to customer satisfaction
Who We Are
Our Values
Environmental, Social and Governance
At our world-class manufacturing and design facility in Ottawa, Ontario, we manufacture rugged products optimized for high-mix, high quality and small batch sizes typical of military requirements. Equipped with the latest assembly, cleaning, coating and inspection equipment, our operations are AS9100 and ISO-9001 certified and we comply with the highest standards of workmanship defined by IPC and J-STD specifications. All materials and processes are controlled by our enterprise-wide SAP and MES systems which offer full component traceability to individual products by serial number.
To learn more visit Ottawa, Ontario | Curtiss-Wright Defense Solutions (curtisswrightds.com)
Head of New Product Development (NPD)
Posted 2 days ago
Job Viewed
Job Description
Head of New Product Development (NPD)
Location: Nationwide (Remote – with up to 50% international travel)
Language: Fluency in English is essential for collaboration across our global teams.
Industry: Aesthetic Medicine, Consumer Health, Cosmetics, and Pharmaceuticals
Seniority Level: Executive Leadership
Reports To : Board of Directors
About the Company
A globally recognized leader in aesthetic treatments and advanced health services is expanding into the consumer product space, launching a high-impact division focused on cosmetics, injectables, and pharmaceuticals. Backed by a renowned clinical reputation and an established international footprint, the company is poised to revolutionize its market presence through cutting-edge product development and brand innovation.
This is a rare opportunity to join an organization at the forefront of science and beauty, where clinical credibility meets visionary product expansion. The Head of NPD will play a pivotal role in shaping this global initiative from the ground up.
Key Responsibilities
Executive Leadership & Strategy
- Define and lead a strategic roadmap for global new product development and market entry
- Report directly to the Board on innovation milestones, brand performance, and commercialization success
Product Innovation & Market Fit
- Guide the research, formulation, clinical validation, and production of innovative health and beauty products
- Bridge scientific insight with consumer needs to ensure strong market resonance
Brand Development & Global Marketing
- Lead brand strategy, messaging, and go-to-market plans across product categories
- Oversee high-profile global product launches and partnerships with major industry players
- Ensure all products align with luxury brand standards and build consumer trust
Commercialization & Distribution
- Develop international distribution networks and go-to-market channels
- Foster relationships with influencer networks, industry KOLs, and strategic partners to amplify reach
Regulatory & Compliance Leadership
- Ensure all products meet regulatory standards in major markets including FDA (US), Health Canada, EMA (Europe), and GCC/MENA authorities
- Oversee safety, efficacy, and documentation for global product compliance
Team Leadership & Culture
- Recruit, lead, and mentor a high-performing global team in NPD, marketing, and commercialization
- Create a culture of excellence, collaboration, and scientific innovation
Qualifications
Education
- Advanced degree (PhD, PharmD, MBA, or equivalent) in Cosmetic Science, Pharmaceutical Sciences, Biotechnology, or a related field
Experience
- 15+ years of executive leadership in product development and brand growth, particularly within beauty, health, or consumer goods sectors
- Proven success in launching global products and managing cross-border regulatory pathways
- Deep commercial understanding of North American and MENA (Middle East/North Africa) markets
Leadership & Cultural Fit
- Board-level communication and reporting experience
- History of building elite cross-functional teams
- International travel readiness (approx. 50%)
- Exceptional interpersonal, negotiation, and cultural fluency
Why Join This Company?
- Gain direct executive visibility and Board-level influence
- Lead the launch of a global division for cosmetics and consumer pharmaceuticals
- Drive innovation at the intersection of science, beauty, and health
- Be part of a rapidly growing and globally recognized organization
- Travel internationally and leave a lasting legacy in one of the world’s fastest-growing industries
About Blue Signal:
Blue Signal is an award-winning, executive search firm specializing in various specialties. Our recruiters have a proven track record of placing top-tier talent across industry verticals, with deep expertise in numerous professional services. Learn more at bit.ly/46Gs4yS
Senior Full Stack Developer - Product Development Group
Posted 2 days ago
Job Viewed
Job Description
Job Description
Company Description
Canadian Bank Note Company (CBN) is a trusted leader in secure technology solutions for governments and businesses worldwide. The company operates across various business domains, including currency production, border security, civil identity, driver identification and vehicle information, excise control, lottery and charitable gaming.
Our 7 Core Principles shape and guide our corporate behaviours and underpin the sense of community you will experience at CBN. We pride ourselves on fostering a supportive and collaborative work environment, where employees are valued for their contributions and encouraged to grow professionally.
At CBN we seek long-term relationships with our employees and recognize and reward them with a competitive total compensation package that includes:
- An industry-leading defined contribution pension plan with company matching contributions (up to 5%) and payment of service fees;
- Best-in-class health, medical, and life insurance benefits;
- Access to virtual and telehealth services and apps; and
- Very progressive fertility, adoption, and surrogacy benefits to support all definitions of family.
Internal Job Title: Software Developer
Job Type: Permanent, Full-Time
Job Location: Ottawa ON
Work Model: Hybrid
Position Summary
As a Senior Full Stack Software Developer in our Product Development group, you will be responsible for designing, developing, and maintaining scalable applications. You will work closely with cross-functional teams including product owners, architects, and other developers to create seamless, efficient and high-quality solutions. Your expertise in both front-end and back-end technologies will be crucial in delivering high-quality, user-centric applications.
Responsibilities
Application Development
- Design and develop applications that are robust, high quality, scalable and maintainable
- Develop and maintain both client-side and server-side components using modern technologies
- Ensure seamless integration between the front-end and back-end components
- Write clean, maintainable, and efficient code while adhering to industry best practices and CBN coding standards
- Use version control systems like Git to manage code changes and collaborate with other developers
- Document code and create technical documentation to ensure maintainability
Technical Leadership & Mentorship
- Conduct thorough code reviews to ensure adherence to best practices.
- Provide technical guidance and mentorship to junior and mid-level developers.
- Advocate for continuous learning and skill development within the team.
- Participate in architectural discussions and provide recommendations.
Troubleshooting & Optimization
- Troubleshoot and debug complex issues across the stack
- Identify and resolve issues in both the front-end and back-end of the application
- Use debugging tools and techniques to diagnose and fix problems
- Conduct performance testing and profiling to identify and resolve bottlenecks
- Ensure the application is highly available and can recover quickly from failures
Collaboration
- Collaborate with product owners, designers, and other developers to understand requirements and provide technical solutions
- Conduct code reviews and review code written by other developers to ensure it meets quality standards
- Provide constructive feedback and suggest improvements to enhance code quality
- Foster a culture of continuous improvement and knowledge sharing within the team
Innovation
- Continuously learn about new technologies and industry trends
- Evaluate and incorporate new tools and technologies that can improve the development process
- Stay informed about best practices and emerging standards in web development
Various Other Duties and Responsibilities
QualificationsEducation and Knowledge
- Bachelor’s degree in Computer Science (or similar field) or equivalent combination of education and years of relevant work experience
- Knowledge of the following:
- Object oriented programming principles
- Three-tier client-server architecture
- Automated testing
- Agile (SCRUM) development methodology
Experience
- 8+ years of software development experience
Technology
- Languages: Java and C#
- Frameworks: Angular
- Databases: PostgreSQL / SQL
- Cloud: Azure/AWS
- Containerization: Docker / Kubernetes
- Automated testing : Junit, Mockito, Karma, Protractor, REST Assured, Robot Framework
- Tools: Jira, Git, ADO
Soft Skills and Competencies
- Critical thinking skills
- Analysis, problem-solving
- Interpersonal skills
- Communication, teamwork and collaboration
- Organization and time management skills
- Growth mindset
- Self-directed
Mandatory Requirements
- Language: Fluency in English
Additional Information
Canadian Bank Note Company (CBN) is committed to fostering a diverse and inclusive workplace where all employees are treated with dignity and respect. We are proud to be an equal opportunity employer and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, veteran status, sexual orientation, gender identity, or any other legally protected status.
We provide equal employment opportunities to all individuals, including women, Indigenous Peoples, persons with disabilities, visible minorities, and members of the 2SLGBTQ+ community. Our commitment to equity extends to all aspects of employment, including recruitment, hiring, promotion, compensation, benefits, training, and development. As part of our commitment to providing an inclusive, barrier free selection process, we ask that if you are contacted regarding the competition for this position, you advise the interview coordinator or any accommodation measures you may require.
At CBN, we value the unique perspectives and experiences that each employee brings to our organization, and we are committed to maintaining a workplace that reflects the diverse communities we serve. We believe that diversity and inclusion drive innovation and success, and we strive to create an environment where every employee can thrive and contribute to our collective goals.
Product Development Manager (Hardware)-Onsite Position - Ottawa, ON

Posted 14 days ago
Job Viewed
Job Description
We're looking for highly motivated **_Product Development Manager (Hardware)_** _t_ o join our **_Ottawa, ON_** team, you will **_lead a dynamic group_** of Hardware Engineers responsible for the development of **_new products and the support of the existing product lines_** . You plan and oversee the product development related activities, ensuring objectives are accomplished to meet the business and customer objectives.
You will also work closely with other cross-functional team members in Engineering, New Product Introduction (NPI), Customer Support, Sales and Marketing. You coach, mentor, guide, and help nurture the development team to realize its full potential and adopt our culture of quality and customer satisfaction.
**Location:** **_Ottawa, ON_**
**We Take Care of Our People**
Paid Time Off **I** RRSP with Employer Match **I** Health and Wellness Benefits **I** Learning and Development Opportunities **I** Competitive Pay **I** Referral Program **I** Recognition **I** Employee Stock Purchase Plan ( **I** Inclusive & Supportive Culture ( *
**Your Challenge**
Supervise the work assignments of a highly knowledgeable and motivated project teams
+ Be a hands-on leader who achieves success through modelling best practices and a service attitude
+ Responsible for the career development, training and performance evaluations of staff allocated to the Engineering Team
+ Facilitate and ensure individual and team roles and responsibilities are understood
+ Establish effective practices to attract, develop, motivate and retain high caliber staff
+ Help lead cross-functional problem-solving initiatives
+ Review testing protocols for compliance with accepted standards and verifies testing results to ensure the desired functionality has been achieved
+ Participate in bid/project activities such as defining architectures, developing technical proposals and providing detailed cost and schedule estimates
+ Interact with customers regarding requirements and technical solutions
+ Manage 3rd party relationships and coordination of work for cross site initiatives
+ Pre- and Post-Sales support when needed by Product Marketing or Customer Support
**What You Bring**
+ Bachelor's Degree in Electrical Engineering or Computer Science, Technologist Diploma or equivalent will be considered
+ 8 years industry experience relating to electronics computing
+ Prior experience in a managerial or leadership role is preferred
+ Experience/familiarity in the following is an asset:
+ Development of electronic assemblies for aerospace applications
+ Design for manufacturing processes and techniques
+ Design for rugged environments
+ Open system standards such as VME, VPX, XMC and PMC
+ Leading-edge Intel and NXP/Qualcomm processors (x86, PA, ARM)
+ Leading-edge Broadcom Ethernet Switches
+ High-end FPGA design
+ Latest embedded industry technologies, such as Gen 3/4 PCI Express, 40GbE Ethernet, USB 3, DDR4 memory, etc.
+ Working knowledge of PCB technologies including stack up definition, material selection, IPC etc.
+ Experience with product configuration management
+ DO-254 Safety Certification
+ Demonstrated drive and ability to achieve goals in an innovative and fast paced environment
+ Demonstrated ability to manage multiple tasks simultaneously and able to react to shifting priorities to meet business need
+ Demonstrated creativity, foresight, and mature engineering judgment in anticipating and solving unprecedented engineering problems
+ The candidate should be a results-oriented team player who leads by example, holds themselves accountable for performance, takes ownership of their responsibilities, and champions process improvement initiatives
+ Self-confident leader capable of motivating and mentoring their staff
+ Ability to estimate/schedule development projects
+ Detailed knowledge of embedded computing systems architecture, hardware, software and related support requirements in the military/aerospace industry
+ Team orientated and commitment to customer satisfaction
**Who We Are**
Our Values ( Social and Governance
At our world-class manufacturing and design facility in Ottawa, Ontario, we manufacture rugged products optimized for high-mix, high quality and small batch sizes typical of military requirements. Equipped with the latest assembly, cleaning, coating and inspection equipment, our operations are AS9100 and ISO-9001 certified and we comply with the highest standards of workmanship defined by IPC and J-STD specifications. All materials and processes are controlled by our enterprise-wide SAP and MES systems which offer full component traceability to individual products by serial number.
To learn more visit Ottawa, Ontario | Curtiss-Wright Defense Solutions (curtisswrightds.com) ( unsolicited agency submittals please. Agency partners must be invited to participate in a search by our_ **_Talent Acquisition Team ( )_** _and have signed terms in place prior to any submittal. Resumes submitted directly to any Curtiss-Wright employee or affiliate will not qualify for fee payment, and therefore become the property of Curtiss-Wright._
**Compliance Statement**
This position may require exposure to export-controlled information and subject to additional security screening. In the event information provided during the security screening reveals ineligibility to access export-controlled information, any offer of employment may be reconsidered or withdrawn.
Curtiss-Wright is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, sexual orientation, gender identity, physical or mental disability, age, ancestry, legally protected medical condition, family care status, marital status, religion, veteran status, national origin, or any other legally protected status. If you require accommodation during the recruitment process, please contact Talent Acquisition. ( )
**For US Applicants: EEO is The Law - click here for more information. ( you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition ( ) and we will make all reasonable efforts to accommodate your request.
**Join the WRIGHT Team!**
Over 95 years of growth, Curtiss-Wright is an integrated, market-facing global diversified industrial company and remains a technology leader through this legacy of innovation. Through three well-balanced segments - Aerospace & Industrial, Defense Electronics and Naval & Power, we remain focused on advanced technologies for high performance platforms and critical applications. Diversity, commitment to excellence and dedication to the spirit of pioneering innovation continue to drive the employees of Curtiss-Wright.
**Our Values**
What makes a world-class organization? It all begins with core values that provide a strong foundation for success. Simple in theory, the values of Curtiss-Wright are reflected in every aspect of our operations. To our employees, these are more than words on a wall - we all take these values to heart in our relationships with our customers and each other.
**Leadership**
We lead based on vision and strategic direction, empowering employees to reach goals through thoughtful and decisive action.
**Customer Focus**
We are committed to achieving total quality by meeting our customers' expectations and delivering products and services in a timely fashion.
**Teamwork & Trust**
Working in a spirit of trust and collaboration, we actively encourage employees to contribute their ideas and innovations to keep our company moving forward.
**Respect for People**
We believe that people are our most valuable asset and will always do the right thing in our dealings and interactions with all employees.
**Integrity**
We will act with the highest integrity in all of our business relationships and strategic partnerships.
**What We Offer Our Employees:**
**Opportunity:** As part of the Curtiss-Wright team, you have the opportunity each day to transform the way customers do business, as well as transform your career. Our entrepreneurial environment provides you with excellent experiences that enable you to develop your skills through stretch assignments and the opportunity to work with the best talent in the industry. You will have the opportunity to contribute from day one!
**Challenging Work:** The work we do here is not only challenging, but it is meaningful to our customers, our employees and the communities in which they live and work. You are given the chance to work on some of the most advanced technology projects in the world. Now that something to be proud of!
**Collaborative Environment:** The teamwork among our exceptionally talented people enables us to deliver some of the most advanced solutions to our customers.
Research Assistant or Research Associate
Posted today
Job Viewed
Job Description
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.
Be The First To Know
About the latest Research and development Jobs in Ottawa !
Sr. Clinical Research Associate - Oncology - Western Canada
Posted 2 days ago
Job Viewed
Job Description
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.
These is a great opportunity for CRA's who are looking to get off the road and work 100% from home. 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 trials remote monitoring only
- Have a minimum of 2 -3 years’ experience in monitoring pharmaceutical industry clinical trials
- Have a minimum of 1-3 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, 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.
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.
Sr. Clinical Research Associate - Oncology - Western Canada
Posted 2 days ago
Job Viewed
Job Description
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.
These is a great opportunity for CRA's who are looking to get off the road and work 100% from home. 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 trials remote monitoring only
- Have a minimum of 2 -3 years’ experience in monitoring pharmaceutical industry clinical trials
- Have a minimum of 1-3 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, 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.
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.
Attaché de recherche clinique II, Oncologie /Clinical Research Associate II, Oncology

Posted 14 days ago
Job Viewed
Job Description
**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