Biosampling Project Leader

GSKMississauga, ON
Hybrid

About The Position

This role will lead biosampling activities for clinical studies in Canada. The successful candidate will design and deliver biosampling and sample logistics plans that protect sample quality and patient safety. This involves close collaboration with study teams, sites, laboratories, and vendors to resolve issues and ensure studies remain on schedule. The ideal candidate is a clear communicator who is organized, collaborative, and practical. This position offers significant opportunities for professional growth, making a meaningful impact, and contributing to GSK’s mission of uniting science, technology, and talent to get ahead of disease together.

Requirements

  • Bachelor’s degree in life sciences, pharmacy, biomedical sciences or related field.
  • At least 3 years practical experience in biosampling, sample management, clinical operations or laboratory support.
  • Hands-on knowledge of sample collection, processing, storage and shipment, including cold chain fundamentals.
  • Working knowledge of Good Clinical Practice and regulatory requirements for clinical samples.
  • Strong organizational skills with experience coordinating multiple tasks and timelines.
  • Proficient in written and spoken English; able to communicate clearly with global and local partners.

Nice To Haves

  • Experience working with central laboratories or bioanalytical vendors on global clinical studies.
  • Familiarity with sample tracking systems or laboratory information management systems (LIMS).
  • Experience with temperature-controlled logistics and use of data loggers for shipments.
  • Experience performing sample quality checks, troubleshooting integrity issues and conducting root cause analysis.
  • Project management training or certification.
  • Advanced degree in a relevant scientific discipline.

Responsibilities

  • Lead design and delivery of biosampling plans, sample handling procedures and logistics for clinical studies in Canada.
  • Coordinate with study teams, clinical sites, central and local laboratories, and logistics partners to ensure consistent sample handling.
  • Maintain chain of custody, correct storage conditions and temperature control for all samples.
  • Monitor timelines and quality metrics, identify risks to sample integrity, and drive corrective actions.
  • Prepare and maintain study-specific biosampling documents, including procedures, work instructions and sample tracking guides.
  • Provide training and support to site staff and study teams on biosampling procedures and quality expectations.

Benefits

  • Opportunities to grow
  • Make meaningful impact
  • Support GSK’s mission
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