Site: The Brigham and Women's Hospital, Inc. At Mass General Brigham, we know it takes a surprising range of talented professionals to advance our mission—from doctors, nurses, business people and tech experts, to dedicated researchers and systems analysts. As a not-for-profit organization, Mass General Brigham is committed to supporting patient care, research, teaching, and service to the community. We place great value on being a diverse, equitable and inclusive organization as we aim to reflect the diversity of the patients we serve. At Mass General Brigham, we believe a diverse set of backgrounds and lived experiences makes us stronger by challenging our assumptions with new perspectives that can drive revolutionary discoveries in medical innovations in research and patient care. Therefore, we invite and welcome applicants from traditionally underrepresented groups in healthcare — people of color, people with disabilities, LGBTQ community, and/or gender expansive, first and second-generation immigrants, veterans, and people from different socioeconomic backgrounds – to apply. Job Summary Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; maintaining and updating data generated by the study. Essential Functions Reviews proposals for compliance with sponsor and organizational guidelines; verify all sponsor requirements are met. Recruiting patients for clinical trials, conducts phone. Verifies the accuracy of study forms and updates them per protocol. Prepares data for analysis and data entry. Documents patient visits and procedures. Assists with regulatory binders and QA/QC Procedures. Assists with interviewing study subjects. Assists with study regulator submissions. Qualifications Education: Bachelor's Degree in Science required. Can this role accept experience in lieu of a degree? Yes. Experience: Some relevant research project work 0-1 year preferred. Knowledge, Skills and Abilities Careful attention to detail and good organizational skills. Ability to follow directions. Good interpersonal and communication skills. Computer literacy. Working knowledge of clinical research protocols. Ability to demonstrate respect and professionalism for subjects' rights and individual needs. Additional Job Details (if applicable) The Cognitive Outcomes of Geriatric Surgery (COGS) Research Group is seeking a responsible, highly motivated, and enthusiastic candidate for the position of Clinical Research Coordinator (CRC) I. Our mission is to understand why surgery and general anesthesia cause both acute and long-lasting cognitive impairment in older adults. As such, we are interested in the impact of common geriatric conditions such as mild cognitive impairment and frailty in the development of postoperative delirium; the role of surgery-induced inflammation on cognitive outcomes; and whether surgery/anesthesia exacerbate occult pre-existing cerebral neurodegeneration. The PIs are NIH-funded clinical anesthesiologists and the multidisciplinary team includes surgeons, neurologists, a neuropsychologist, scientists expert in biomarker analysis and discovery, and statistician / bioinformatician. Working under the general supervision of the PIs, the CRC is responsible for managing and executing our clinical research studies according to established policies and procedures. This includes recruiting and evaluating patients; collecting and organizing patient data; performing pre- and postoperative clinical screening such as memory and delirium testing; drawing blood samples; processing blood samples for biomarker assays; running selected assays; maintaining and updating data generated by the study; scheduling patients for follow-up study visits and calls; preparing and amending IRB applications; and adhering to regulatory requirements.
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