Clinical Trial Manager

Assignment DetailsWorkload: ~20 hours/week to start (likely to increase)Engagement: Consulting/contractStart: ASAPLocation: 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 RoleLead identification and evaluation of clinical trial sites across Europe and/or the USDevelop and implement patient recruitment strategies and realistic study timelinesOversee trial documentation, TMF accuracy, regulatory files, and site communicationProvide 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 needsSupport vendor oversight, site readiness, and operational risk managementWhat You BringStrong background in Clinical Trial Management within biotech, pharma, diagnostics, or imagingDemonstrated experience moving programs from Phase 2 to Phase 3Experience with diagnostic agents, peptides, radiopharma, or complex modalities is highly advantageousSolid understanding of EU and US regulatory frameworks, start-up processes, and site operationsAbility to work independently, provide senior-level guidance, and operate in a lean environment