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Project Manager Biotech Jobs in Burnaby, BC (NOW HIRING)

Project Manager

Vancouver, BC

CA$143K - CA$161K/yr

You hold a Bachelor's or Master's degree in Biotech, Life Sciences, Engineering, Project Management, or a related field. * Experience: 4-6+ years of progressive project/program management experience ...

Partnering with Clinical Project Managers (CPMs) to translate global recruitment targets into ... We are a clinical-stage biotechnology company focused on discovering and developing antibody-based ...

Research Scientist

Vancouver, BC · On-site

CA$65K - CA$90K/yr

Sc) in pharmaceutical, biotech or similar industry, directly related to working on DMPK studies ... management skills including the ability to support and prioritize multiple projects Job ...

... medicine for biotechnology, life sciences, pharmaceutical companies and academia partners ... Responsible and accountable for leading projects that directly impact their department, which ...

Country Manager

Vancouver, BC · On-site +1

CA$150K - CA$175K/yr

... biotechnology? At Leica Microsystems, one of Danaher's 15+ operating companies, our work saves ... Here, you will work on meaningful projects alongside passionate colleagues, driving progress and ...

Environmental Specialist

Burnaby, BC · On-site

CA$83K - CA$125K/yr

Proven ability to manage cross-functional projects and interpret regulatory requirements with ... based biotechnology company that helps power leading-edge life science research around the world.

Working closely with cost centers and project leads building forecasts and guiding your teammates ... Supporting our monthly management reporting and quarterly forecasting processes, identifying risks ...

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Project Manager Biotech information

What does a project manager in biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a project manager in biotech?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.

How does a project manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

What job categories do people searching Project Manager Biotech jobs in Burnaby, BC look for?

The top searched job categories for Project Manager Biotech jobs in Burnaby, BC are:

What cities near Burnaby, BC are hiring for Project Manager Biotech jobs?

Cities near Burnaby, BC with the most Project Manager Biotech job openings:

Infographic showing various Project Manager Biotech job openings in Burnaby, BC as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution.

CA$143K - CA$161K/yr

Full-time

Re-posted 26 days ago


Job description

We are seeking a highly motivated and skilled Project Manager to join our Technical Operations team in beautiful Vancouver, BC. Reporting to the Chief Technical Operations Officer, you will support the development and implementation of a project management system and support planning, documenting, tracking and reporting of our programs. You'll be joining a company committed to developing regenerative medicines that deliver life-changing, functional cures for patients living with serious diseases. 

Responsibilities 

  • Supporting the development and implementation of a centralized Project Management System to support planning, documenting, tracking, reporting and when necessary, escalation of team and working group activities, issues, and risks.
  • Supporting the project planning process within established governance structure, monitors progress, and drives execution.
  • Assessing and continuously improving current communication/reporting/tracking tools for effectiveness, efficiency, and ease of use.
  • Developing awareness of industry standard project management structure and tools and assesses appropriateness. When needed, refine Aspect's framework against these standards based on size of company and stage of asset development.
  • Ensuring alignment and codification of all required activities into project logs and to track progress against targeted timelines.
  • Supporting issue resolution and drives risk identification, assessment and mitigation planning including adequate documentation/follow-up of ongoing issues and risks.
  • As required, designing and maintaining reporting of project management activities via tools such as dashboards, slides etc.
  • Facilitating required communications via meeting scheduling, agenda development, and follow-up activities. 
  • Providing support to overall program management activities including presenting content development, participation in management meetings to prepare minutes/actions and providing follow-up, as necessary.
  • Developing and utilizing decision support models, Gantt charts, and timelines to enable achievement of goals.
  • Other duties as assigned.

Qualifications & Experience

  • Education: You hold a Bachelor's or Master's degree in Biotech, Life Sciences, Engineering, Project Management, or a related field. 
  • Experience:  4-6+ years of progressive project/program management experience within a biotech, pharmaceutical, or scientific R&D environment.
  • Lifecycle Experience: Proven hands-on track record driving therapeutic programs past the Development Candidate (DC) stage, through GLP studies, and successfully into First-in-Human (FIH) clinical trials or beyond. 
  • Cross-Functional Influence: Demonstrated success in influencing multidisciplinary scientific/technical teams and managing complex, cross-functional initiatives without direct authority.
  • Strategic Partnership: Ability to drive critical decisions, manage timelines, and partner seamlessly with Program Technical Leads to meet overarching corporate goals.
  • Creative Problem Solving: You love immersing yourself in difficult technical problems and coming up with solutions that work. You think outside the box and use your experience and intuition to identify when such solutions are realistic.
  • Operational Rigor: Outstanding attention to detail, strong organizational skills, and a commitment to process rigor. 
  • Execution & Delivery: You have outstanding attention to detail and take pride in your work. You can multitask, prioritize competing deadlines, and have a track record for delivering work on time.

The hiring range for this role is $143,852 - $161,834, annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job-related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above-range offers. Note that base salary is just one part of the overall compensation at Aspect. Members of the Aspect team also receive equity, a comprehensive benefits package, and support for continuous learning and career progression