Central Laboratory Vendor/Project Manager - Remote - FSP
reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in reputed company do.
Each 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 recruiting 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 quality 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 strategy
Some specifics about this advertised role
Supports individual clinical study teams as required for reputed company technical and operational sample-reputed company matters for assigned projects by liaising with internal stakeholders, such as working with Informed Consent Form (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 well 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 human sample acquisition projects
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 Human Sample Management team to ensure reputed company samples transferred to internal research groups are documented, tracked, used and destroyed.
Who are reputed company
reputed company supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client 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 the well-being of many patients.
You’ll be an influential 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 well-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 academic, CRO or pharmaceutical/biotech industry. We are seeking a professional 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 section, Protocol review for samples section, blood volume calculations, lab reputed company build), to initiation, maintenance and study reputed company-out