Freshers Clinical Research Job at Mass General Brigham, USA | Apply Online & Earnb Upto $37.86 /hr

Interested in research that combines participant interaction, clinical assessments and data management? This Clinical Research Coordinator Job at Massachusetts General Hospital’s Center for Addiction Medicine welcomes new graduates for consideration at the Clinical Research Coordinator I level. Based in Boston, the position supports multi-year studies, including community-based and imaging research.

  • Position: Clinical Research Coordinator – Center for Addiction Medicine

  • Location: 101 Merrimac Street, Boston, Massachusetts, USA

  • Grade: 5

  • Requisition ID: RQ4085678

About the Organisation

The Center for Addiction Medicine conducts clinical research at Massachusetts General Hospital. This position supports studies involving participant recruitment, psychiatric assessments, neuropsychological testing and imaging, with activities taking place in the laboratory and at external study sites.

Clinical Research Coordinator Job: Role Overview

Working independently and under general supervision, the coordinator will help organize study activities and carry out participant-facing procedures. Responsibilities include scheduling, recruitment, assessments, adverse-event monitoring and database quality assurance.

Candidates will be considered for CRC I or CRC II according to their experience.

Key Responsibilities

In this Clinical Research Coordinator Job, CRC I duties include:

  • Recruit and schedule participants, conduct interviews and verify study eligibility.

  • Explain studies and, where assigned, obtain informed consent.

  • Administer and score questionnaires and support psychiatric and neuropsychological assessments.

  • Collect information from participants, medical records and physicians.

  • Document visits, maintain databases and prepare graphs and reports.

  • Perform assigned study procedures, which may include phlebotomy.

  • Support adverse-event monitoring, regulatory submissions and consent-form preparation.

  • Maintain regulatory binders and assist with quality assurance and quality control.

  • Conduct literature searches and provide administrative support.

CRC II responsibilities may additionally include data analysis, recruitment strategy development, protocol recommendations and contributions to annual reviews and study reports.

Education and Experience

  • Bachelor’s degree required.

  • CRC I: New graduates with relevant coursework or project experience, as well as applicants without prior research experience, will be considered.

  • CRC II: Candidates with one to two years of directly related experience will be considered.

  • Bilingual applicants are preferred, but bilingual proficiency is not required.

CRC I has no supervisory responsibility.

Skills Required

Candidates should demonstrate strong organization, attention to detail, computer literacy and clear communication. The ability to follow study protocols and respect participants’ rights and individual needs is essential.

CRC II candidates should also bring analytical skills, data interpretation capabilities and familiarity with data management programs.

Pay and Benefits

The posting lists an hourly range of $20.16–$37.86 (midpoint $29.01), with actual base pay depending on skills, experience and education.

The posting describes comprehensive benefits, career development and recognition programs, with differentials, premiums or bonuses where applicable.

For graduates interested in participant-focused research, this Clinical Research Coordinator Job offers an opportunity to build skills in study coordination, assessments and research documentation. Bring your curiosity, careful judgment and respectful approach to a team conducting addiction medicine studies.

APPLY ONLINE HERE