Pharmaron in Baltimore, MD seeks a Trial Master File Specialist to keep TMFs compliant, complete, and inspection-ready throughout the study lifecycle. You will own TMF management, develop filing strategies, and support audits with CRAs and sponsors.
The role requires 5+ years in TMF/clinical document management in CRO/biopharma, a Bachelor’s or Associate degree, and strong knowledge of ICH-GCP and eTMF systems. On-site work with competitive benefits and career growth opportunities.
#J-18808-LjbffrTMF Compliance Specialist — eTMF Expert in baltimore at Unknown Company
This position is listed as full time and onsite.