- 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
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Clinical Research Coordinator I - Worcester - UMass Med School
Description
Clinical Research Coordinator IMinimum Salary
US-MA-Worcester
Job Location
1 week ago(2/24/2026 9:11 PM)
Requisition Number
# of Openings
1
Posted Date
Day
Shift
Non Exempt
Exempt/Non-Exempt Status
Non Union Position -W60- Non Unit Professional
Position Type
Full-Time
Min
USD $40,000.00/Yr.
Max
USD $48,000.00/Yr.
Overview
POSITION SUMMARY:
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.
Our research team conducts an array of studies related to addressing social disparities and perinatal and pediatric care. We work with directly with families with social disadvantage, including families with limited English proficiency, families of minoritized race/ethnicity, and those with low-income. We do an array of clinical and health services research using qualitative and quantitative methods. We do observational and interventional studies. We are seeking a Clinical Research Coordinator to join our growing, passionate research team and work under the direction of the Principal Investigator (PI) or designee. Tasks will involve a large array of 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. Our team is seeking a highly motivated individual with an interest in social determinants of health and addressing disparities in healthcare.
ResponsibilitiesESSENTIAL FUNCTIONS:
- Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
REQUIRED QUALIFICATIONS:
Fluent in Spanish preferred
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Clinical Research Coordinator
Only for registered members Worcester
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Research Nurse Coordinator
Only for registered members Worcester
-
Clinical Research Coordinator
Only for registered members Worcester, Massachusetts, United States
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Clinical Research Coordinator
Only for registered members Worcester
-
Clinical Research Coordinator
Only for registered members Worcester
-
Research Nurse Coordinator
Only for registered members Worcester, Massachusetts, United States
-
Clinical Research Coordinator
Only for registered members Worcester, MA
-
Research Nurse Coordinator
Full time Only for registered members Worcester
-
Research Nurse Coordinator
Full time Only for registered members Worcester
-
Research Nurse Coordinator
Full time Only for registered members Worcester
-
Clinical Research Coordinator
OTHER Only for registered members Worcester
-
Clinical Research Coordinator
Only for registered members Worcester, MA
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Clinical Research Coordinator
Full time Only for registered members Worcester
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Clinical Research Coordinator I
Only for registered members Worcester
-
Clinical Research Coordinator II
Only for registered members Worcester
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Clinical Research Coordinator II
Only for registered members Worcester
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Clinical Research Coordinator I
Only for registered members Worcester
-
Clinical Research Coordinator II
Only for registered members Worcester
-
Clinical Research Coordinator II
Only for registered members Worcester, Massachusetts, United States
-
Clinical Research Coordinator I
OTHER Only for registered members Worcester
-
Clinical Research Coordinator I
OTHER Only for registered members Worcester