Clinical Research Coordinator

GENERAL SUMMARY/ OVERVIEW STATEMENT: The Massachusetts General Hospital Department of Psychiatry is seeking a full-time, bilingual (English/Spanish) Clinical Research Coordinator I to assist with the operation of current, ongoing research studies as well as assist with the operation of future studies. Primary responsibilities include implementing study protocols, administering neuropsychological tests to elderly subjects with or without cognitive problems, maintaining accurate documentation, and assisting with other research tasks as needed. We are seeking a highly motivated clinical research coordinator with strong interpersonal skills necessary to interact with elderly subjects. The ideal applicant should have the drive and enthusiasm to be an integral part of a team that is working to better understand aging and neurodegenerative diseases. The CRC I will help with recruiting and undertake scheduling and all the visit tasks described above for Spanish-speaking participants. PRINCIPAL DUTIES AND RESPONSIBILITIES: Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position. 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 SKILLS/ABILITIES/COMPETENCIES REQUIRED: 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 EDUCATION: Bachelor's degree required. EXPERIENCE: New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above. Candidates with more experience can be hired as a CRC II if appropriate.