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Clinical Research Coordinator

Mass General Brigham
Somerville, United Statesfull_timeVerifiedPosted 29 Sept 2025
💰 $56,880/yr($39,520/yr$56,880/yr)

About the role

Site: The General Hospital Corporation


 

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.


 

Massachusetts General Hospital (MGH) Biostatistics is seeking several Clinical Research Coordinators to join our team working on the National Institutes of Health (NIH) sponsored RECOVER project, an initiative to understand, prevent, and treat the long-term complications of SARS-CoV-2 infection. Mass General Brigham (MGB) is partnering with the NIH to launch the RECOVER Data Resource Core (DRC), which will contribute to the collection, harmonization, and quality assurance of data collected on study participants, including so-called COVID-19 “long-haulers,” throughout the nation. This team will operate under a Principal Investigator based at MGH. We are looking for a well-organized, dynamic, and highly motivated Clinical Research Coordinator to join MGH Biostatistics to support conduct of the Data Coordinating Center functions of the RECOVER project. The Clinical Research Coordinator will report to the Project Manager and will work closely with biostatisticians, data managers, and study staff to support study operations, data collection and quality control, and reporting of research findings. Strong organizational, communication, and problem-solving abilities in a fast-paced research environment are required.
Role Specific Responsibilities:
- Participate in all phases of research projects, from conception and design of studies through proofing manuscripts for submission to academic journals
- Monitor study activities for compliance with all applicable regulations and facilitate trainings for study personnel as needed
- Partner with collaborators and study staff across sites on oversight of studies, standard operating procedure development and review, and data quality assurance
-Assist in preparation of posters and slides for presentation at research conferences
- Support preparation progress reports, applications, and related documents
- Organize group meetings, including setting up conference calls and taking minutes


 

Job Summary

Summary
Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelor's degree have a grace period of six months from their hire date (up to 1 year if starting per diem) to provide degree equivalency verification.

Does this position require Patient Care?
No

Essential Functions
-Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met.

-Recruiting patients for clinical trials, conducts phone interviews.

-Verifies the accuracy of study forms and updates them per protocol.

-Prepares data for analysis and data entry.

-Documents patient visits and procedures.

-Assists with regulatory binders and QA/QC Procedures.

-Assists with interviewing study subjects.

-Assists with study regulator submissions.


 

Qualifications

Education

Bachelor's Degree Science required

Experience
Some relevant research project work 0-1 year preferred

Knowledge, Skills and Abilities
- 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.


 

Additional Job Details (if applicable)

Additional Job Description


 

Remote Type

Hybrid


 

Work Location

399 Revolution Drive


 

Scheduled Weekly Hours

40


 

Employee Type

Regular


 

Work Shift

Day (United States of America)



 

Pay Range

$19.76 - $28.44/Hourly


 

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Company

Mass General Brigham

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