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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