Clinical Research Coordinator I

Mass General Brigham is a not-for-profit organization dedicated to advancing patient care, research, teaching, and community service. They are seeking a Clinical Research Coordinator (CRC) to assist with studies in the Department of Psychiatry/Behavioral Medicine, focusing on psychosocial interventions for chronic illness. The CRC will collaborate with a multidisciplinary research team while managing various responsibilities related to participant recruitment and study operations.

Responsibilities

• Oversee and coordinate the recruitment, enrollment, and study visits of research participants
• Maintains records and databases
• Performs administrative support duties as required
• Carry out study visits involving interviews and surveys
• Coordinates operations of clinical research activities such as study documentation, reporting, & logistics
• Act as a point of contact for the study
• Train new study staff and trainees
• Participate in qualitative and quantitative data analysis
• Participate in manuscript writing and submission
• Other responsibilities include maintaining participant databases, purchasing study supplies, leading and/or participating in weekly team/departmental meetings, and other various administrative tasks

Skills

• High school diploma, GED or equivalent
• Proficiency with Microsoft-based software such as Excel, Word, PowerPoint, and Outlook to process data and enhance communication
• Strong interpersonal skills and comfort working with people
• Affirming and nondiscriminatory attitudes and behaviors towards all people
• Careful attention to detail
• Good organizational and time management skills, with the ability to prioritize
• Adherence to protocol and regulatory guidelines
• This position requires a high degree of motivation and self-sufficiency, although extensive training will be provided
• Ability to problem solve effectively and independently
• Oversee and coordinate the recruitment, enrollment, and study visits of research participants
• Maintains records and databases
• Performs administrative support duties as required
• Carry out study visits involving interviews and surveys
• Coordinates operations of clinical research activities such as study documentation, reporting, & logistics
• Act as a point of contact for the study
• Train new study staff and trainees
• Participate in qualitative and quantitative data analysis
• Participate in manuscript writing and submission
• Other responsibilities include maintaining participant databases, purchasing study supplies, leading and/or participating in weekly team/departmental meetings, and other various administrative tasks
• Bachelor's degree, ideally in public health/psychology or related fields
• Previous clinical research experience including work with research participants, collection of clinical data (surveys), using REDCap databases, or familiarity with IRB requirements and regulatory documentation is beneficial but not required
• Lived experience, education, research experience, advocacy, and community organization experience will all be considered as beneficial background for this position

Benefits

• Comprehensive benefits
• Career advancement opportunities
• Differentials
• Premiums and bonuses as applicable
• Recognition programs designed to celebrate your contributions and support your professional growth

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