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Bioanalytical Project Manager Jobs in Vancouver, BC

Frontage Laboratories

Research Scientist

Vancouver, BC · On-site

CA$65K - CA$90K/yr

... non-regulated bioanalytical (various platforms including LC/MS/MS and MSD for small and large ... management skills including the ability to support and prioritize multiple projects Job ...

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Bioanalytical Project Manager information

What does a bioanalytical project manager do?

A Bioanalytical Project Manager oversees and coordinates bioanalytical studies, ensuring that projects are completed on time, within budget, and according to regulatory standards. They act as the main point of contact between clients, laboratory teams, and regulatory agencies, managing study timelines, resources, and data quality. Their responsibilities include planning project activities, monitoring progress, troubleshooting issues, and reporting results to stakeholders. They play a critical role in drug development by ensuring that bioanalytical testing meets scientific and compliance requirements.

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

To thrive as a Bioanalytical Project Manager, you need a strong background in bioanalysis, project management experience, and typically a degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (such as GLP/GCP), and project management tools like MS Project is essential. Excellent communication, leadership, and organizational skills help manage cross-functional teams and client expectations. These skills ensure the successful planning, execution, and delivery of complex bioanalytical projects within regulatory and timeline constraints.

What are some common challenges faced by bioanalytical project managers, and how can they be addressed?

Bioanalytical Project Managers often face challenges coordinating timelines across multiple stakeholders, such as laboratory teams, clients, and regulatory bodies. Managing shifting project priorities and ensuring data integrity under tight deadlines can also be demanding. To address these challenges, effective communication, proactive risk management, and strong organizational skills are essential. Regular status meetings, clear documentation, and building strong relationships with both internal and external partners help keep projects on track and ensure compliance with regulatory standards.

What is the difference between Bioanalytical Project Manager vs Bioanalytical Scientist?

AspectBioanalytical Project ManagerBioanalytical Scientist
CredentialsBachelor's or Master's in Life Sciences, PMP often preferredDegree in Biology, Chemistry, or related field; PhD or Master's common
Work EnvironmentProject teams, client meetings, coordination rolesLaboratory research, data analysis, method development
Employer & Industry UsagePharmaceutical, biotech companies, CROsResearch labs, pharmaceutical companies, CROs

The Bioanalytical Project Manager oversees project timelines, budgets, and client communication, ensuring successful completion. In contrast, the Bioanalytical Scientist focuses on experimental design, data collection, and method development. Both roles are essential in the bioanalytical industry but differ in responsibilities and daily tasks.

What are popular job titles related to Bioanalytical Project Manager jobs in Vancouver, BC?

For Bioanalytical Project Manager jobs in Vancouver, BC, the most frequently searched job titles are:

What job categories do people searching Bioanalytical Project Manager jobs in Vancouver, BC look for?

The top searched job categories for Bioanalytical Project Manager jobs in Vancouver, BC are:

Bioanalytical Project Manager jobs near you
Infographic showing various Bioanalytical Project Manager job openings in Vancouver, BC as of June 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

Research Scientist

Frontage Laboratories

Vancouver, BC • On-site

CA$65K - CA$90K/yr

Full-time

Re-posted 19 days ago

Key responsibilities

  • Plan and execute in vitro and in vivo metabolism/bioanalysis assays.

  • Perform data analysis, interpretation, and prepare study summaries.

  • Participate in assay/method development, troubleshooting, and provide scientific input.

Job description

 


Job Title: Research Scientist, DMPK (Regular, full-time)

Job Location: Vancouver, BC 

Salary: $65,000-$90,000/year, salary commensurate with experience


Frontage is a global Contract Research Company (CRO) with the head office located in Exton, Pennsylvania, USA. Frontage has 25 sites across USA, Canada, China and Italy. The Canadian operations include two sites – one located in Vancouver and the other based in Toronto. Frontage Vancouver (formerly BRI) has been in operation for more than 25 years with service offerings in regulated and non-regulated bioanalytical (various platforms including LC/MS/MS and MSD for small and large molecules analyses), In-vitro / In-vivo Drug Metabolism & Pharmacokinetics and pharmacology. The Frontage Vancouver operation is projected to grow significantly in the next few years, especially to meet the demands of biotech and pharmaceutical companies in the Pacific Northwest region. Our facility is accredited by AAALAC and conforms to GLP standards.


This position requires teamwork and excellent oral and written communication skills with a strong understanding in DMPK and applied techniques.


Skills and Qualifications:

  • Requires a B.Sc or M.Sc. in pharmaceutical sciences, chemistry, biochemistry or other science related discipline.
  • A minimum of 5 years’ experience for B.Sc (or 3 years for M.Sc) in pharmaceutical, biotech or similar industry, directly related to working on DMPK studies.
  • Demonstrated experience in contemporary HPLC and LC-MS/MS operation, method development and troubleshooting.
  • Experience with developing and optimizing relevant DMPK assays.
  • Hands-on technical experience with tissue culture, automated liquid handlers, and MSD platform preferred.
  • Prior experience with radioisotope handling (e.g. 3H, 14C) is an asset.
  • Competence in experimental in vitro and in vivo study design supporting ADME/DMPK/Tox preclinical and clinical studies
  • Hands-on experience with preparing formulations.
  • Strong planning and organization abilities. 
  • Competent and self-motivated individual with the ability to work collaboratively and independently under moderate supervision in a fast-paced, matrixed team environment.
  • Good verbal and written communication skills.
  • Strong computers skills, and competent in using MS Word, MS Excel, Graphpad Prism, and WinNonlin.
  • Good analytical, logical thinking and problem-solving skills, and the ability to adapt to changing priorities and deadlines.
  • Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects


Job Responsibilities:

  • Report to senior team leader
  • Plan and execute in vitro and in vivo metabolism/bioanalysis assays in a team-oriented environment
  • Perform data analysis and interpretation using different software programs (such as Sciex Analyst, Sciex OS, MassLynx, GraphPad prism, LIMS, MS Excel, etc.) and prepare study summaries
  • Participate in assay/method development, troubleshooting, and provide scientific input
  • Coordinate with study team members to execute studies and lead studies when required
  • Communicate and work closely with department leads to complete projects in a timely manner
  • Prepare study protocols and study reports
  • Liaison /communicate results proficiently with study sponsors
  • Provide drug discovery screening and IND filling support for Sponsor-based projects
  • Ensure that all applicable regulations, guidelines and BRI standard operating procedures are followed
  • Responsible and reliable record keeping, organization and assisting in lab management as needed.
  • Ensure that all study related documentation is completed and archived as required.
  • Contribute to basic lab maintenance such as equipment maintenance / cleaning, supply ordering, stocking, and follow-up
  • Follow safety policies and procedures.
  • Ability to lift 35 lbs.


Frontage is an Equal Opportunity Employer and provides equal opportunities to all employees. 

We respect and seek to empower each individual and support the diverse cultures, perspectives, skills and experiences within our workforce. All employment is decided on the basis of qualifications, merit and business need.

We thank all applicants for their interest; however, only candidates under consideration will be contacted.