Clinical Research Coordinator I

Company:  University of Massachusetts Medical School
Location: Worcester
Hours: Full Time
Type: Permanent
Job Requirements / Description

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.


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, interviews, and tests

Coordinate participant remuneration/compensation per protocol

Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors

Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance

Document and collect data and/or samples for research related procedures performed during participant study visits.

Ensure clinicians and/or PI accurately document their study activities according to protocol

Track and maintain study enrollment and completion of milestones

Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe.

Track and maintain study related information in the data management system within the required timeframe

Responsible for monitoring the inventory of research related supplies

Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs

Present study status reports related to assigned research projects

Participate in the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)

Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.

Comply with all safety and infection control standards appropriate to this position

Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives

Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices

Must practice discretion and adhere to school and hospital confidentiality at all times

Perform other duties as required.


Bachelor’s degree in a scientific or health related field, or equivalent experience

0-1 year of related experience

Ability to travel off site locations

Additional Information:
Highly Desired:





IRB submissions

Ability to multitask

Organizational skills


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