Seeking a talented Clinical Document Management Associate/Specialist for a really exciting biotech company in California with an advanced clinical pipeline in a number of indication areas. The role can be conducted fully remote but the candidate needs to be based in California:
Clinical document management, TMF, or site regulatory documentation experience preferred
Maintain eTMF, ensuring tracking of essential study documents and periodic quality reviews to assure accuracy and completeness.
Supports daily activities of the eTMF systems
Manages the workflow for document review, collection, metadata entry, upload and inventory
This is a long-term, 40 hour per week w2 assignment (8+ months initial contract) with good potential to convert to FTE. You would be eligible for a good hourly rate, health/dental/vision/401k and sick pay (no PTO).