Clinical Research Coordinator

Mass General BrighamBoston, MA
Hybrid

About The Position

This full-time Clinical Research Coordinator position at Massachusetts General Hospital, part of Mass General Brigham, focuses on research into self-injury and depression among youth. The role involves assisting with NIMH- and American Foundation for Suicide Prevention-funded studies aimed at improving short-term risk prediction for suicidal behavior in adolescents. These studies utilize computational methods to model neurocognitive markers and ambulatory indices (including mobile technology like actigraphy, passive sensing of physiological arousal, social engagement, physical activity, and ecological momentary assessment) in psychiatrically hospitalized youth. Additionally, some studies employ computer vision to identify visual indicators of suicide risk in adolescents. The coordinator will work under the mentorship of Dr. Richard Liu and Dr. Taylor Burke. This position is particularly well-suited for individuals seeking to gain research and clinical experience before pursuing graduate or medical school.

Requirements

  • Careful attention to details
  • Good organizational skills
  • Ability to follow directions
  • Good communication skills
  • Computer literacy
  • Working knowledge of clinical research protocols
  • Ability to demonstrate respect and professionalism for subjects’ rights and individual needs
  • Bachelor's degree
  • Strong writing skills

Nice To Haves

  • Prior research or clinical experience is strongly recommended
  • Psychology and majors in related areas are encouraged to apply

Responsibilities

  • Collects & organizes patient data
  • Maintains records and databases
  • Uses software programs to generate graphs and reports
  • Assists with recruiting patients for clinical trials
  • Obtains patient study data from medical records, physicians, etc.
  • Conducts library searches
  • Verifies accuracy of study forms
  • Updates study forms per protocol
  • Documents patient visits and procedures
  • Assists with regulatory binders and QA/QC procedures
  • Assists with interviewing study subjects
  • Administers and scores questionnaires
  • Provides basic explanation of study and in some cases obtains informed consent from subjects
  • Performs study procedures, which may include phlebotomy
  • Assists with study regulatory submissions
  • Writes consent forms
  • Verifies subject inclusion/exclusion criteria
  • Performs administrative support duties as required
  • Opportunities to conduct independent research, submit presentations to national conferences, and prepare manuscripts for publication

Benefits

  • Comprehensive benefits
  • Career advancement opportunities
  • Differentials
  • Premiums
  • Bonuses
  • Recognition programs
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