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The Clinical Research Coordinator supports multi-year clinical research studies within the Division of General Internal Medicine at Massachusetts General Hospital. The coordinator works independently and under the general supervision of the study Principal Investigator, Dr. Joanna Streck, and Senior Program Manager, Michele Reyen. Responsibilities include patient scheduling and recruitment, subject-oriented study procedures, questionnaire administration, adverse-event monitoring, protocol-related administration, database management, and quality assurance. The role follows established policies, procedures, and study protocols and supports study recruitment, evaluation, consent, data collection and maintenance, and regulatory activities. This position does not require patient care. It is onsite at 100 Cambridge Street, with a 40-hour work week on the day shift. The coordinator may collect data through focus groups, qualitative interviews, self-report surveys, and biological data; design data collection instruments; maintain study data using REDCap or other programs; prepare reports and IRB documentation; correspond with the IRB and other regulatory groups; and assist with manuscripts, grants, and conference presentations. The role also provides general administrative support and may involve working with undergraduate research interns who volunteer on study projects. Candidates must be fluent in English and interested in learning about studies in diverse medical and community settings, including work with vulnerable populations and people affected by challenging life stressors or medical illness.
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Job Type
Full-time
Career Level
Entry Level

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