remote Full-time

Parexel is hiring a Global Trial Manager - Central Laboratory - FSP - Remote - Immediate Start

About the Role

Parexel is hiring a Global Trial Manager to ensure the quality of samples and data delivered to support biomarker and non-biomarker evaluation for global clinical studies. This role is central to maintaining protocol adherence and resolving sample-related issues through close collaboration with project managers, CTMs, and CROs.

What You'll Do

  • Support individual clinical study teams for all technical and operational sample-related matters by liaising with internal stakeholders.
  • Establish, oversee, plan, and integrate all issues related to collection, processing, storage, shipping, transfer, and reporting/billing of samples and data.
  • Provide guidance to clinical teams and sites regarding collection, storage, and shipping of samples from clinical trials.
  • Work with scientists and clinical teams to ensure sample collection and usage complies with study protocol and applicable Informed Consent Forms.
  • Work closely with the internal Human Sample Management team to ensure all samples transferred to internal research groups are documented, tracked, used, and destroyed.
  • Assist with resolving any sample-related issues or queries.
  • Provide overall project management in alignment with the core business strategy.

What We're Looking For

  • 6-8 years of clinical research experience within an academic, CRO, or pharmaceutical/biotech industry setting.
  • Working knowledge of clinical trials and clinical databases.
  • Oncology experience is mandatory.
  • Vendor coordination experience (e.g., Central Lab, specialty lab, CROs).
  • Prior experience supporting clinical trials from set-up (ICF review, Protocol review, blood volume calculations, lab kit build) through initiation, maintenance, and study close-out.

Nice to Have

  • Laboratory sample management experience.
  • Preference for solid tumour experience.
  • Haemato-oncology experience is acceptable.

Team & Environment

You will work closely with project managers (central and/or specialty labs), clinical trial management (CTM), the CRO, and other internal stakeholders.

Work Mode

This is a remote position, open to candidates located in the UK and Europe.

Parexel is an equal opportunity employer.

Required Skills
Clinical Trial ManagementCentral Laboratory OperationsICH-GCPProject ManagementVendor ManagementStakeholder CommunicationBudget ManagementRegulatory Compliance
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About company
Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

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Job Details
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Posted 8 months ago