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Biostatistical Programmer (m/f/d)
About the Role: A leading global pharmaceutical company is seeking an experienced freelance biostatistical programmer to support a pivotal Phase 3 clinical trial. This is a contract-based opportunity ideal for professionals with strong statistical programming skills and prior submission experience.Key Responsibilities:Support the integration of new...
Freelance Clinical Research Associate
EPM Scientific are currently partnered with a Mid-Sized CRO running a global project in Oncology. They are urgently seeking a Freelance Clinical Research Associate (CRA) to support their expanding clinical operations team. See a short summary below: Contract Conditions:Start date: ASAPLocation: Portugal, RemoteContract Type: Freelance / Consultant ...
Validation Engineer
We have a current opportunity for a Validation Engineer on a contract basis. The position will be based in Ireland. For further information about this position please apply.Key Responsibilities:Lead and support validation activities including development of Validation Master Plans and execution of IQ/OQ/PQ protocols.Collaborate with contract manufa...
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QC Validation Scientist
QC Validation Scientist Location: Geneva Area Workload: 100% Start Date: ASAP Contract Duration: Until 31.08.2027In this role, you'll lead analytical and validation activities to ensure compliance with pharmaceutical quality standards.Ideal for an experienced scientist with a strong background in raw material analysis, process validation, and regul...
Category Manager
Freelance Opportunity: Category Manager - Biotech (R&D Procurement) đź“Ť Location: Brussels, Belgium (Hybrid) đź“… Start Date: ASAP đź“„ Contract Type: Freelance | 12 months | Full-timeAbout the Role A leading biotech company in Brussels is looking for an experienced Freelance Category Manager to support its R&D procurement function. You'll lead strategi...
CSV Consultant
Please note: Applicants must hold an EU passport or existing right to work in the EU (no sponsorship available). Fluency in French or Dutch is mandatory.A leading pharmaceutical/biotech organisation is seeking an experienced Computer System Validation (CSV) Consultant to support critical projects in compliance with GAMP 5 guidelines. This role offe...