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
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