Clinical Research Coordinator

Mass General Brigham • Boston, MA

5d • $21 - $29 • Onsite

About The Position

The Clinical Research Coordinator I assists with human research and associated laboratory work in collaboration with numerous departments. Following established policies, procedures, and study protocols, the coordinator supports clinical research studies, including recruiting, evaluating, and consenting patients; collecting and organizing patient data; scheduling study visits; performing clinical tests such as phlebotomy and EKGs; and maintaining study data. The role provides quality assurance and administrative support for clinical protocols. Under the direction of the Clinical Research Program/Project Manager, the coordinator works with clinical and research team members to help ensure enrollment goals and study procedures are met, and serves as a liaison to participating clinic staff and study team members. Patient care is not required.

Requirements

• Bachelor's degree in a related field of study, or qualifying experience in lieu of a degree.
• Careful attention to detail and good organizational skills.
• Ability to follow directions.
• Good interpersonal and communication skills.
• Computer literacy.
• Working knowledge of clinical research protocols.
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Nice To Haves

• Some relevant research project work; 0–1 year preferred.

Responsibilities

• Review proposals for compliance with sponsor and organizational guidelines and verify that sponsor requirements are met.
• Recruit patients for clinical trials and conduct phone interviews.
• Verify the accuracy of study forms and update them according to protocol.
• Prepare data for analysis and data entry.
• Document patient visits and procedures.
• Assist with regulatory binders and quality assurance and quality control procedures.
• Assist with interviewing study subjects.
• Assist with study regulatory submissions.
• Support recruitment, evaluation, and consenting of patients for studies.
• Collect and organize patient data, schedule study visits, perform clinical tests such as phlebotomy and EKGs, and maintain and update study data.
• Provide quality assurance and administrative support for clinical protocols.
• Serve as a liaison between participating clinic staff and study team members.

Benefits

• Comprehensive benefits.
• Career advancement opportunities.
• Differentials, premiums, and bonuses as applicable.
• Recognition programs designed to celebrate contributions and support professional growth.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level