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

Summary: Mass General Brigham is a not-for-profit organization that supports patient care, research, teaching, and community service. They are seeking a Clinical Research Coordinator I to work within the Pediatric Neurotherapeutics and Psychopharmacology Clinical and Research Program, contributing to research studies focused on mental health disorders in children. The role involves managing patient data, assisting with clinical trials, and communicating with the Institutional Review Board. 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 Required Qualifications: - 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 Required Skills: Clinical trials experience, Data collection, organization, Regulatory submissions Important Skills: Patient recruitment, Database management Nice-to-Have Skills: Communication skills, Attention to detail, Problem-solving Benefits: Comprehensive benefits, Career advancement opportunities, Differentials, Premiums, Bonuses, Recognition programs designed to celebrate your contributions and support your professional growth