Clinical Research Coordinator - Center for Genomic Medicine

Massachusetts General Hospital
United States, Massachusetts, Boston
185 Cambridge Street (Show on map)
Apr 07, 2025
The Sweetser Laboratory in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) and the MGH Medical Genetics Program is seeking a motivated, enthusiastic candidate to join our research group. This position would entail providing: Assistance with maintaining the MGH Genetics Biorepository for Rare Genetic Disorders oConsenting patients and curation of samples oMaintaining records and updating the RedCap database oMedical records abstraction oAssisting in IRB amendments and reviews oCreation of clinical survey instruments oAssisting in preparing data for publications Assistance with coordination of patient evaluations for the Undiagnosed Diseases Network (UDN) and the MGH Rare and Undiagnosed Diseases Program oCoordinate consent process between patients and family members and the site genetic counselor/coordinator oCoordinate the distribution and collection of consent forms, release forms, blood collection kits oAssist genetic counselor in requesting and compiling medical records oAssist genetic counselor in organizing research evaluations oAssist with tracking and data entry for the HUND, including data entry in RedCap database oAssist with clinical and research billing oManage processing of storing, tracking, and shipping samples, both clinical and research 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. PRINCIPAL DUTIES AND 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 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. SUPERVISORY RESPONSIBILITY (if applicable): A Clinical Research Coordinator I does not have any supervisory responsibility. The General Hospital Corporation is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.