Clinical Research Coordinator II

Mass General Brigham•Boston, MA

1d•Hybrid

About The Position

The Center for Precision Psychiatry (CPP) at Massachusetts General Hospital is seeking applications for a full-time Clinical Research Coordinator (CRC) to coordinate and administer projects led by Dr. Matthew Nock aimed at better understanding short-term suicide risk and evaluating innovative interventions to prevent suicidal behaviors. This position is particularly well-suited for individuals interested in pursuing graduate training in psychology, public health, medicine, or related fields. The CRC will join a collaborative, multidisciplinary research team and play an integral role in the day-to-day execution of several studies. Responsibilities will include, but are not limited to, supporting study start-up activities, participant recruitment and screening, REDCap database management and survey administration, longitudinal participant follow-up via text, phone call, and email, coordination of study documentation, assistance with IRB submissions and correspondence, and other project-related administrative and research activities. This role offers exposure to many aspects of clinical research and provides opportunities to work closely with investigators, clinical partners, and research staff across multiple settings. We view the CRC as an important member of our team and are committed to providing mentorship and professional development opportunities. The position will involve working alongside colleagues at MGB, Harvard, and affiliate hospitals (e.g., Brigham and Women’s Faulkner Hospital). This variety provides a unique opportunity to gain experience across academic, clinical, and community-based research environments.

Requirements

Bachelor's Degree Science required
Related post-bachelor's degree research experience 1-2 years required
Ability to work more independently and as a team member.
Computer literacy, analytical skills, and ability to resolve technical problems.
Ability to interpret the acceptability of data results.
Working knowledge of data management programs.

Nice To Haves

Experience working with clinically severe or suicidal populations
Strong interpersonal skills
Excellent organizational, writing, and computer skills
Experience with ecological momentary assessment
Experience with statistical software
Experience with research databases
Prior supervision and leadership responsibilities

Responsibilities

Supports study start-up activities.
Participant recruitment and screening.
REDCap database management and survey administration.
Longitudinal participant follow-up via text, phone call, and email.
Coordination of study documentation.
Assistance with IRB submissions and correspondence.
Other project-related administrative and research activities.
Assists with determining the suitability of study subjects and acts as a resource for patients and families.
Has input into recruitment strategies and may contribute to protocol recommendations.
Administers scores and evaluates study questionnaires.
Maintains research data, patient files, regulatory binders, and study databases.
Performs data analysis and QA/QC checks and organizes and interprets data.
Assists with preparation for annual review and assists PI in completing study reports and presentations.
May assist with training and orientation of new staff members.