Clinical Research Coordinator I
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 various research and advocacy projects aimed at assisting families impacted by substance use disorder, including participant recruitment, data collection, and preparing grant progress reports.
Responsibilities
- Assists in development of study protocols including consent forms, interview guides, survey development, recruitment strategies, and data collection plans with staff and study investigators
- Assists with Institutional Review Board (IRB) applications, continuing reviews, and amendments
- Supports participant recruitment and data collection, such as verifying eligibility inclusion/exclusion criteria, supporting interview or focus group procedures, and administering surveys and questionnaires for research and reporting requirements
- Coordinates and organizes meetings related to grant activities. Develops agendas and documents discussion through detailed meeting notes
- Obtains patient study data and maintains records and databases
- Prepares data for analysis and data entry
- Prepares grant performance reports on specified measures
- Supports qualitative and quantitative data analysis
- Assists in literature review and manuscript preparation
- Contribute to protocol recommendations
- Organize, interpret, and monitor data
- Serves as a study resource for participants and families, ensuring communication is clear, respectful, and aligned with trauma-informed care principles
- Other duties as assigned
Skills
- Bachelor's Degree Related Field of Study required
- Basic understanding of disease model of substance use disorder, medications for opioid use disorder, working with underserved populations
- Proficiency in various software packages, including Microsoft Office, NVivo, REDCap, and other desktop tools
- Working knowledge of data management and statistical software (including SAS, R, or STATA)
- Careful attention to detail and good organizational skills
- Ability to follow directions
- Good interpersonal and communication skills
- Computer literacy
- Working knowledge of clinical research protocols
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs
- Some relevant research project work 0-1 year preferred
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses
- Recognition programs designed to celebrate your contributions and support your professional growth
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