Clinical Research Coordinator I - Launch Your Research Career

Mass General Brigham; Boston (MA); Hybrid; USD 29,000 - 40,000; Full time

Job summary

Mass General Brigham in Boston invites applications for a Clinical Research Coordinator supporting clinical trials across hospital sites. Under supervision, you will screen and recruit participants, coordinate data collection, and help run tests as needed.

You will work with Principal Investigators and RCNet/CCI teams, manage study documentation, and ensure protocol compliance. This hybrid role is based at 221 Longwood Avenue with a 40-hour work week.

Qualifications

• BS OR BA required, equivalent experience or research certification acceptable as well.
• Some knowledge of medical terminology, clinical practice and/or research studies highly desired.
• Sound independent judgment and willingness to learn competence in research methodologies a must.

Responsibilities

• Coordinate implementation of sponsored clinical research studies.
• Initiate and maintain recruitment contact with study participants.
• Screen applicants, ensuring they meet criteria and assess suitability for participation.
• May perform clinical tests such as phlebotomy, ECGs, etc.
• Collaborate with PI/Research Manager and senior coordinators to develop recruitment strategies.
• Assist RCNet/CCI teams with administrative duties integral to programs.
• Interact with patients, provide education, and support follow-up.
• Maintain and validate study data and assist in data entry into CRFs as applicable.
• Input data and assist with basic analyses and reporting as needed.
• Support regulatory paperwork for IRB approval and protocol communications.

Skills

Independent work

Interpersonal skills

Communication skills

Analytical skills

Computer literacy

Organizational skills

Attention to detail

Professionalism

Data management knowledge

Education

BS OR BA

Job description

Mass General Brigham in Boston invites applications for a Clinical Research Coordinator supporting clinical trials across hospital sites. Under supervision, you will screen and recruit participants, coordinate data collection, and help run tests as needed.

You will work with Principal Investigators and RCNet/CCI teams, manage study documentation, and ensure protocol compliance. This hybrid role is based at 221 Longwood Avenue with a 40-hour work week.