On-site TMF Master File Specialist | Regulatory Expert
Listed on 2026-10-01
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Pharmaceutical
Healthcare Compliance, Regulatory Compliance Specialist, Medical Science Liaison
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
The On-site TMF Master File Specialist | Regulatory Expert role at Pharmaron Beijing Co. Ltd. is now open for applications in Baltimore, MD, United States.
We are looking to fill the On-site TMF Master File Specialist | Regulatory Expert position at Pharmaron Beijing Co. Ltd. in Baltimore, MD, United States.
Join us at Pharmaron Beijing Co. Ltd. as our next On-site TMF Master File Specialist | Regulatory Expert in Baltimore, MD, United States.
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