Pharmaron is seeking a Trial Master File Specialist to ensure TMFs are compliant, complete, and inspection-ready for clinical trials in Baltimore, MD on-site. You will own sponsor TMFs from study start-up through closeout, develop TMF plans, and act as the SME for eTMF systems, ensuring adherence to ICH-GCP and CDISC TMF standards.
The role requires strong attention to detail, excellent organizational and communication skills, and the ability to manage multiple studies in a fast-paced
#J-18808-LjbffrOn-site TMF Master File Specialist | Regulatory Expert in baltimore at Unknown Company
This position is listed as full time and onsite.