Global eTMF Specialist: Documentation & Compliance Optimizer
Planet Pharma
Planet Pharma is seeking an eTMF Specialist to manage and optimize the electronic Trial Master File (eTMF) for global clinical trials. The role involves ensuring that clinical documentation is accurate and compliant, while supporting trials from initiation to close-out phases. The ideal candidate will have a Bachelor’s degree in Life Sciences or Business Administration, with 1-2 years of experience in clinical trial documentation. Key skills include strong communication, organization, and analytical abilities. The position offers dynamic challenges in a collaborative environment. #J-18808-Ljbffr Planet Pharma
Vacancy posted 3 days ago
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