Sr. Clinical Research Coordinator
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. Job Summary Working independently and following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; and maintaining and updating data generated by the study. Additionally, provide input into determining study subject suitability, input into recruitment strategy, methodology design, statistical analyses, protocol design, and manuscript writing. The ideal candidates have interventional research (drug and/or device) experience and experience with federally funded investigator-initiated trials.
Requirements
- Bachelor's Degree Related Field of Study required, Master's degree preferred (experience can be considered in lieu of a degree)
- At least 3-5 years of related post-bachelor's degree research experience required
- Ability to work more independently and as a team member.
- High degree of computer literacy and analytical skills.
- Ability to identify both technical and non-technical problems and develop solutions.
- Ability to interpret the acceptability of data results.
- Highly proficient data management skills and working knowledge of data management systems.
- Able to display initiative to introduce innovations to research study.
- Excellent time management, organizational, interpersonal, written, and verbal communication skills.
Nice To Haves
- Interventional research (drug and/or device) experience highly preferred
- Experience with Federally funded Investigator Initiated trials is highly preferred
Responsibilities
- Independently determines the suitability of study subjects.
- Develops and implements recruitment strategies.
- Participates in the design of research methodology.
- Plans, performs, and designs statistical analyses.
- Recommends protocol changes, writes protocols, and contributes to manuscripts.
- Independently performs specialized projects.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
