Clinical Research Coordinator I at Mass General Brigham in Boston, MA

Summary: Mass General Brigham is a not-for-profit organization dedicated to advancing patient care, research, teaching, and community service. The Clinical Research Coordinator I will support research activities within the MGH Center for the Neuroscience of Psychedelics, including recruiting and screening study participants, collecting and analyzing data, and maintaining documentation. Responsibilities: - Coordinates the screening and recruitment of study patients - Assists with study regulatory submissions to the MGB IRB and FDA - Collects & organizes patient data - Maintains records and databases - Uses software programs to generate graphs and reports - Assists with recruiting patients for research trials - Obtains patient study data from medical records, physicians, etc - 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, EKGs and running MRI scans - Writes consent forms - Verifies subject inclusion/exclusion criteria - Performs administrative support and other duties as required Required Qualifications: - Coordinates the screening and recruitment of study patients - Assists with study regulatory submissions to the MGB IRB and FDA - Collects & organizes patient data - Maintains records and databases - Uses software programs to generate graphs and reports - Assists with recruiting patients for research trials - Obtains patient study data from medical records, physicians, etc - 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, EKGs and running MRI scans - Writes consent forms - Verifies subject inclusion/exclusion criteria - Performs administrative support and other duties as required - Must be self-motivated, mature, and responsible with excellent organizational, as well as oral and written communication skills - Must be able to work independently in a dynamic environment - Must be able to juggle and prioritize multiple tasks - Must feel comfortable working with clinical and non-clinical study populations - Must seek assistance when appropriate Required Skills: Clinical research coordination, Study participant recruitment, Study screening, Regulatory submissions, IRB submissions, FDA submissions, Data collection, Data organization, Database management, Software for graph, report generation, Medical record data extraction, Study form verification, Protocol adherence, Regulatory binder management, Quality assurance, Quality control, Interviewing study subjects, Questionnaire administration, Informed consent, Phlebotomy, Electrocardiogram (EKG), MRI scan operation, Consent form writing, Inclusion/exclusion criteria verification, Administrative support Benefits: Comprehensive benefits, Career advancement opportunities, Differentials, Premiums and bonuses, Recognition programs designed to celebrate your contributions and support your professional growth