Remote: Veeva Vault Study Documentation Specialist

A leading pharmaceutical company is seeking a Study Documentation Specialist to support a team in managing GLP/GCP research study documents. In this role, you will handle classification and compliance using Veeva Vault, while closely collaborating with internal teams and CROs. The contract is freelance for 1 year with a strong chance of extension. Candidates with CRO experience are preferred, and strong EU-based profiles may work remotely. Attention to detail and document management experience are essential. #J-18808-Ljbffr