Clinical Trials Regulatory Coordinator
Listed on 2026-10-17
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Pharmaceutical
Healthcare Compliance, Regulatory Compliance Specialist
Tufts Medicine seeks a Regulatory Project Manager to complete regulatory requirements for clinical research projects under the direction of investigators and a Clinical Research Regulatory PM.
You will coordinate protocol submissions, prepare regulatory documents, and maintain records to ensure compliance with Tufts Medical Center policies, federal regulations, and ICH/GCP guidelines. Collaborates with NCCCR and external partners to manage amendments and reporting.
We are looking to fill the Clinical Trials Regulatory Coordinator position at Tufts Medicine in Boston, MA, United States.
Join Tufts Medicine and contribute to our ongoing work.
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This posting is for the Clinical Trials Regulatory Coordinator role at Tufts Medicine, based in Boston, MA, United States.
The Clinical Trials Regulatory Coordinator role at Tufts Medicine is now open for applications in Boston, MA, United States.
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