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UMass Chan Medical School is seeking a Clinical Research Coordinator to independently perform delegated tasks and procedures involving human subject research under the direction of a Principal Investigator or designee. The role coordinates regulatory activities, participant visits, data and sample collection, study documentation, compliance, and research operations across multiple open-rank levels, while also support

Responsibilities Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data Conduct preliminary quality assurance reviews of s