Remote Clinical eTMF Specialist, Compliance & Audits

CryoLife, Inc.

Remote job

Artivion, Inc. is seeking a Clinical eTMF Specialist to manage the electronic Trial Master File across clinical trials, ensuring GCP/ICH compliance and inspection readiness. You will collaborate with cross-functional teams, CROs, and study sites to maintain accurate, complete documentation in eTMF systems. Responsibilities include QC, indexing, training, and supporting regulatory inspections, with travel as required. Prior TMF/eTMF experience and knowledge of ICH-GCP FDA EMA is required. #J-18808-Ljbffr CryoLife, Inc.

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Vacancy posted 6 days ago

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