Clinical Trial Manager

1 week ago

Uxbridge, United Kingdom Parexel Full time

Clinical Trial Manager - Central Laboratory Vendor Manager - Remote - FSP - Immediate Start Parexel, Uxbridge, England, United Kingdom We are currently recruiting an experienced Central Labs Project Manager to join one of our key sponsors in Europe. The role is based in the UK but involves working on global studies. Key responsibilities include ensuring that quality samples and data are delivered to support biomarker and non‑biomarker evaluation and enable 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 CROs to ensure samples are collected per protocol and assist with resolving any sample‑related issues or queries. Additional responsibilities include overall project management in alignment with the core business strategy. Some Specifics About This Advertised Role Supports individual clinical study teams as required for all technical and operational sample‑related matters for assigned projects, liaising with internal stakeholders such as the Informed Consent Form (ICF) specialist. Establishment, oversight, planning, and integration of all issues related to collection, processing, storage, shipping and transfer of samples and data, as well as reporting/billing for study‑related operations. Provides guidance to clinical teams and sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other human sample acquisition projects. Works with scientists and clinical teams to ensure sample collection and usage is in compliance with study protocol and applicable ICF. Works closely with the internal Human Sample Management team to ensure all samples transferred to internal research groups are documented, tracked, used and destroyed. Who Are Parexel Parexel supports clinical studies across the full range of therapeutic areas and has longstanding partnerships with a vast client base. We supported the trials of most of today’s top 50 best‑selling drugs, and we also enable more niche drug developments that are critical to many patients. You’ll be an influential member of the wider team. What We Are Looking For In This Role For every role, we look for professionals who have the determination and courage to put patient well‑being first. That to us is working with heart. Requirements Specific to This Role 6‑8 years clinical research experience with academic, CRO, or pharmaceutical/biotech industry. Working knowledge of clinical trials and clinical databases is required. Central Laboratory Management experience is essential. Oncology experience is mandatory; preference for solid tumours, Haemato‑oncology experience acceptable if solid and traceable across multiple phases (I‑III). Vendor coordination experience (e.g., Central Lab, specialty lab, CROs, etc.). Prior experience supporting clinical trials from setup (ICF review/drafting for sample sections, protocol review for sample sections, blood volume calculations, lab kit build) to initiation, maintenance and study close‑out. Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Health Care Provider, Science, and Research Industries Pharmaceutical Manufacturing, Biotechnology Research, Hospitals and Health Care #J-18808-Ljbffr

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