Research Technician II
About The Position
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. This position enrolls eligible patients to clinical research protocols and manages data collection and regulatory submissions for multiple cancer studies. It serves as the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. The position involves a high volume of data abstraction and data entry.
Requirements
- Bachelor's Degree in a related field of study required
- 1-2 years of related research experience required
- Ability to work independently and as a team member
- Good organization and communication skills
- High degree of computer literacy
- Proficient analytical skills and ability to resolve problems
- Ability to interpret acceptability of data results
- Careful attention to detail
- Working knowledge of clinical research protocols
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs
Responsibilities
- Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all criteria
- Enroll patients as required by the study sponsor and internal enrollment monitor team
- Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance
- Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulations
- Maintain research charts and/or electronic files for all enrolled patients
- Communicate protocol clarifications from the study sponsor
- Schedule and prepare for monitoring visits and audits
- Collect, complete, and submit essential regulatory documents and protocol information to various regulatory entities (IRB)
Benefits
- Comprehensive benefits
- Career advancement opportunities
- Differentials
- Premiums
- Bonuses
- Recognition programs
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
