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Clinical Research Coordinator

2 weeks ago

Toronto, Ontario, Canada University of Massachusetts Medical School Full time
Job Description

The Clinical Research Coordinator II plays a pivotal role in the success of human subject research at the University of Massachusetts Medical School. Reporting to the Principal Investigator or designee, this individual is responsible for independently performing delegated tasks and procedures involving complex research protocols.

  • Obtain consent from research participants in accordance with IRB-approved protocols and applicable regulations, including HIPAA.
  • Schedule and/or conduct participant study visits, tests, and interviews/telephone follow-up calls.
  • Ensure accuracy and completion of regulatory documentation, including local or central IRB and study data.
Key Responsibilities

The Clinical Research Coordinator II will be responsible for:

  • Presenting study status reports related to assigned research projects.
  • Contributing to data presentations and Institutional Review Board (IRB) processes.
  • Tracking and maintaining study-related information in the data management system within required timeframes.
  • Providing detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs.
  • Contribute to the design, development, and documentation of study-related data and collection tools, such as questionnaires, treatment data, and therapeutic checklists.
Qualifications

To be successful in this role, the ideal candidate will possess:

  • A Bachelor's degree in a scientific or health-related field or equivalent experience.
  • 1-3 years of related experience.
  • Ability to travel to off-site locations.