Clinical Research Coordinator I

Mass General Brigham is a not-for-profit organization that supports patient care, research, teaching, and community service. The Clinical Research Coordinator I (CRC I) will contribute to research studies focused on mental health disorders in children, working under the supervision of the Program Director and in collaboration with other key personnel. Responsibilities Collect & organize patient data Maintain records and databases Use software programs to generate graphs, reports and slide sets Manage the recruitment of patients for research trials Obtain patient study data from medical records, physicians, etc Verify accuracy of study forms Update study forms per protocol Document patient visits and procedures Maintain regulatory binders according to current QA/QC procedures Interview study subjects Administer and score questionnaires Provide basic explanation of study and in some cases obtain informed consent from subjects Perform study procedures, which may include phlebotomy, running MRI scans, and PET scans Assist with study regulatory submissions Draft consent forms and protocols Verify subject inclusion/exclusion criteria Assist with manuscript writing and submission Perform administrative support duties as required Perform other duties as assigned Skills Self-motivated, mature, and responsible Excellent organizational skills Excellent oral and written communication skills Excellent attention to detail Ability to work independently in a dynamic environment Ability to juggle and prioritize multiple tasks Comfortable working with clinical and non-clinical study populations Ability to seek assistance when appropriate Initiative to solve problems Experience working in clinical trials (valued but not required) Collect & organize patient data Maintain records and databases Use software programs to generate graphs, reports and slide sets Manage the recruitment of patients for research trials Obtain patient study data from medical records, physicians, etc Verify accuracy of study forms Update study forms per protocol Document patient visits and procedures Maintain regulatory binders according to current QA/QC procedures Interview study subjects Administer and score questionnaires Provide basic explanation of study and in some cases obtain informed consent from subjects Perform study procedures, which may include phlebotomy, running MRI scans, and PET scans Assist with study regulatory submissions Draft consent forms and protocols Verify subject inclusion/exclusion criteria Assist with manuscript writing and submission Perform administrative support duties as required Perform other duties as assigned Benefits Comprehensive benefits Career advancement opportunities Differentials Premiums and bonuses as applicable Recognition programs designed to celebrate your contributions and support your professional growth Company Overview Mass General Brigham specializes in providing medical treatments and health diagnostics services. It was founded in 1994, and is headquartered in Somerville, Massachusetts, USA, with a workforce of 10001+ employees. Its website is Company H1B Sponsorship Mass General Brigham has a track record of offering H1B sponsorships, with 77 in 2025, 61 in 2024, 93 in 2023, 70 in 2022, 80 in 2021, 29 in 2020. Please note that this does not guarantee sponsorship for this specific role.