Clinical Research Coordinator II

University of Massachusetts Medical School; Worcester (MA); On-site; USD 48,000 - 56,000; Full time

Benefits offered by this job

Paid time off

Medical, dental, and vision coverage

Participation in a retirement plan

Job summary

A prestigious medical institution in Worcester is seeking a Clinical Research Coordinator II. This role involves coordinating human subject research, ensuring compliance with regulatory requirements, and maintaining data management. Candidates should have a Bachelor's degree in a scientific field and 1-3 years of related experience. A hybrid work model is offered, with a competitive salary range of $48,000–$56,000.

Qualifications

• 1-3 years of related experience required.

Responsibilities

• Obtain consent of research participants.
• Ensure accuracy of all regulatory documentation.
• Conduct quality assurance reviews of study data.

Skills

Ability to travel off-site locations

Regulatory documentation accuracy

Data management skills

Education

Bachelor's degree in a scientific or health-related field

Job description

Clinical Research Coordinator II

Job Number: 2025-48848

Category: Research

Location: Worcester, MA

Shift: Day

Exempt/Non-Exempt: Exempt

Business Unit: UMass Chan Medical School

Department: School - Populat & Quantitive Hlth Sci - W455000

Job Type: Full-Time

Union Code: Non Union Position -W60- Non Unit Professional

Num. Openings: 1

Post Date: Nov. 5, 2025

Work Location: Hybrid

Salary Minimum: USD $48,000.00/Yr.

Salary Maximum: USD $56,000.00/Yr.

Position Summary

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II 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 complex research protocols related to treatment, ancillary services, and prevention practices.

Essential Functions

• 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 study data
• Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
• Present study status reports related to assigned research projects
• Contribute to data presentations and Institutional Review Board (IRB) processes
• Track and maintain study related information in the data management system within the required timeframe Provide 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, (e.g. questionnaires, treatment data and/or therapeutic checklists)
• Responsible for monitoring the inventory of research related supplies
• Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
• Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
• Comply with all safety and infection control standards appropriate to this position
• Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.

Required Qualifications

• Bachelors degree in a scientific or health related field, or equivalent experience
• 1-3 years of related experience
• Ability to travel off site locations

Posting Disclaimer

This job posting outlines the primary responsibilities and qualifications for the role but is not intended to be an exhaustive list. Duties and expectations may evolve in response to the needs of the department and the broader institution.

In alignment with our commitment to pay transparency, the base salary range for this position is listed above (exclusive of benefits and retirement). At UMass Chan Medical School, final base salary offers are determined based on a combination of factors, including your skills, education, and relevant experience. We also consider internal equity to ensure fair and consistent compensation across our teams.

Please note that the range provided reflects the full base salary range for this position. Offers are typically made within the midrange to allow for future growth and development within the role.

In addition to base pay, UMass Chan offers a comprehensive Total Rewards package, which includes paid time off, medical, dental, and vision coverage, and participation in a 401(a)-retirement plan, with the option to contribute to a voluntary 403(b) plan.

UMass Chan welcomes all qualified applicants and complies with all state and federal anti-discrimination laws.