Clinical Trial Manager

il y a 2 semaines


Luik, Belgique Discover International Temps plein

Assignment Details Workload: ~20 hours/week to start (likely to increase) Engagement: Consulting/contract Start: ASAP Location: Belgium (hybrid; on-site ideally once per week) Clinical Trial Manager (Consultant) – Phase 3 Diagnostic Development | Belgium (Hybrid) We are supporting a diagnostics-focused biotech seeking an experienced Clinical Trial Manager (CTM) to guide a peptide-based diagnostic product through late-stage development. This is a part-time consulting role with scope to increase as the trials advance. The Role Lead identification and evaluation of clinical trial sites across Europe and/or the US Develop and implement patient recruitment strategies and realistic study timelines Oversee trial documentation, TMF accuracy, regulatory files, and site communication Provide strategic guidance on Phase 3 planning (country selection, site feasibility, regulatory pathways) Advise from a CDMO/technical operations perspective to ensure alignment with manufacturing and regulatory needs Support vendor oversight, site readiness, and operational risk management What You Bring Strong background in Clinical Trial Management within biotech, pharma, diagnostics, or imaging Demonstrated experience moving programs from Phase 2 to Phase 3 Experience with diagnostic agents, peptides, radiopharma, or complex modalities is highly advantageous Solid understanding of EU and US regulatory frameworks, start-up processes, and site operations Ability to work independently, provide senior-level guidance, and operate in a lean environment


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