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Strong fit if you like detail-heavy document control in clinical research, can work independently remotely in the UK, and care about audit-ready TMF quality more than patient-facing or lab work.
As a remote Trial Master File Representative at Celerion, your day centers on keeping essential clinical-trial documents complete, current, and audit-ready in the eTMF. Expect intake and QC of study records, chasing missing or outdated artifacts with study teams, applying TMF reference-model filing rules, and supporting inspection readiness for a pharma-services environment where multi-study document quality is core to delivery.
Build strength in eTMF platforms, ICH GCP document expectations, TMF Reference Model structure, and precise QC of essential documents. Practice clear written follow-up with CRAs, study managers, and vendors; no paid certification list was supplied for this posting.
Yes. The listing is remote, based in the UK.
Celerion is a pharmaceutical services company involved in clinical research and bioanalytical laboratory work; recent news also covers ownership-change activity and Zurich lab expansion.
No specific certification resources or costs were provided for this posting; GCP familiarity and TMF document-control experience are the practical focus.
Website: celerion.com
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Trial Master File Representative - Celerion - Remote (UK) About This Position Celerion, a leading drug research company, is seeking a Trial Master File Representative to join our dynamic team. This role will be based remotely within the UK and involves preparing and maintaining comprehensive Trial Master Files for both internal and external studies. Core Duties Create and maintain structured Trial Master Files that comply with protocol and regulatory requirements. Communicate effectively with client sponsors, project managers, monitors, sites, and other study contacts to ensure compliance. Ensure the completeness and accuracy of all trial documentation within the TMF. What We're Looking For Full and permanent right to work in the UK. Experience in clinical research or a related field is preferred. Strong organizational skills with attention to detail. Excellent communication and interpersonal skills. Familiarity with regulatory requirements for clinical trials. About the Company Celerion is a performance-driven drug research company operating in robust and growing markets. We offer a competitive salary in a strong developmental environment where every employee contributes to making a distinctive impact on global health and well-being. Our team thrives on a sense of purpose, working together to drive innovation and excellence. Applying for This Role Celerion is an equal opportunity employer committed to diversity and inclusion. To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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