Global eTMF Specialist: Trial Documentation & Compliance
Planet Pharma Group
Planet Pharma Group is seeking an eTMF Specialist in Boston, Massachusetts to manage and optimize the electronic Trial Master File (eTMF) for global clinical trials. This role involves ensuring compliance, conducting quality reviews, and supporting clinical trials from start to finish. The ideal candidate has a bachelor's degree in Life Sciences or Business Administration, with 1-2 years of experience in clinical trial documentation. Strong organizational and communication skills are essential for maintaining quality and compliance in clinical documentation. #J-18808-Ljbffr Planet Pharma Group
Vacancy posted 4 days ago
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