New

Clinical Research Coordinator II

Massachusetts General Hospital
United States, Massachusetts, Boston
55 Fruit Street (Show on map)
Aug 11, 2025
General Summary/Overview Statement: The Clinical Research Coordinator II works independently under general supervision to provide support to both our Severe Immunotherapy Complications (SIC) and Termeer Center for Targeted Therapy. This position is a 50% split supporting both programs and our joint mission to develop novel treatments for patients with advanced cancers and transform how we prevent, detect, and manage the serious side effects. The position includes close collaboration with dedicated scientists and clinicians. This position requires clinical skills such as consenting patients to biospecimen collection protocols, as well as laboratory responsibilities of blood, tissue, fluid procurement, processing, and shipping. The CRC II will be trained on the institutional and federal regulations governing clinical research. Principal Duties and Responsibilities: The position represents an individual able to perform the following job duties independently under general supervision by the Clinical Research Manager: Identify, approach, and consent patients for participation in research Organize biospecimen collection from patients in both outpatient and inpatient settings (not actual phlebotomy) Develop protocol specific flow charts, intake sheets, and other tools as needed to ensure protocol compliance and proper data acquisition Collect and input data necessary for patient enrollment and registration Maintain a central database (REDCap) of collected samples with appropriate clinical information (clinical demographics, clinical data) Interact with other clinical and laboratory researchers at MGH and other institutions to coordinate analysis of collected samples Requires going to biopsy procedures to help harvest tissue for research Involves sample processing, shipping and banking Involves attending autopsies to collect samples for research Interface in a professional manner with patients as well as a diverse team of physicians, clinical research assistants, nurses, and pathologists Attend lab research and disease group team meetings Skills/Abilities/Competencies Required Careful attention to detail 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 BA/BS degree required Experience Minimum of 1-2 years of related experience or completion of the CCPO New Staff Orientation Program including completion of competency assessment. Supervisory Responsibilities None Working Conditions Duties will primarily be performed in an ambulatory/clinical office setting 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.