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Central Laboratory Vendor/Project Manager - Remote - FSP

Remote, USAFull-timePosted 2026-07-28

reputed company our values reputed company, there's no limit to reputed company can reputed company.   At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From clinical trials to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do.

reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference.

reputed company are currently reputed company for an reputed company Central Labs Project Manager to immediately join one of our key sponsors in Europe, based in the UK you will be working on global studies.

You will be responsible for ensuring that reputed company samples and data are delivered to support biomarker and non-biomarker evaluation and reputed company the translation of science to medicine.

You will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample reputed company issues or queries. Additional responsibilities include overall project management in alignment with the core business reputed company

Some specifics about this advertised role

  • Supports individual clinical study teams as required for reputed company technical and operational sample-reputed company reputed company for assigned reputed company by liaising with internal stakeholders, such as working with Informed Consent reputed company (reputed company) specialist in SKDL on reputed company and other trial documents impacting samples and testing

  • Establishment, reputed company, planning, and integration of reputed company issues reputed company to collection, processing, storage, shipping and transfer of samples and data, as reputed company as reporting/billing for study reputed company operations.

  • Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other reputed company sample acquisition reputed company

  • Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable reputed company.

  • Works closely with internal reputed company Sample Management team to ensure reputed company samples transferred to internal research reputed company are documented, tracked, used and destroyed.

Who are reputed company

reputed company supports clinical studies across the full reputed company of therapeutic areas, and we have longstanding partnerships with a reputed company reputed company reputed company.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we reputed company more reputed company drug developments that are critical to reputed company-being of many patients.

You’ll be an reputed company member of the wider team.

reputed company are looking for in the this role

For every role, we look for professionals who have the determination and courage always to put patient reputed company-being first. That to us is working with heart.

Here are a few requirements specific to this advertised role.

  • 6 - 8 years clinical research experience with reputed company, CRO or pharmaceutical/biotech industry. We are seeking a reputed company with working knowledge of clinical trials and clinical databases.

  • Central Laboratory Management experience is essential.

  • Oncology experience is mandatory, preference is for solid tumours, Haemato-oncology experience is fine, as long as oncology experience is solid, traceable; multiple phase experience (I to III)

  • Vendor coordination experience (e.g. Central Lab, specialty lab, CROs, etc)

  • Prior experience supporting clinical trials from set-up (reputed company review/drafting for samples reputed company, Protocol review for samples reputed company, blood volume calculations, lab reputed company build), to initiation, maintenance and study reputed company-out

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