Senior 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. Under the general direction of the Principal Investigator and Research Nurse Manager, the Senior Clinical Research Coordinator serves as a lead team member, subject matter expert and trial coordinator. Designs, implements, and coordinates both industry and physician sponsored research trials. This includes acting as a liaison between the Principal Investigator, clinical collaborators, the study sponsor, clinical trial regulatory groups (IRB, FDA, etc.), and other research staff to ensure adherence to the study protocols. Implements the research protocol through study closeout and ensures data validation, regulatory compliance, and quality control. 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.; 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.
Requirements
- A minimum of 3-5 years of clinical research experience is required.
- Computer proficiency in MS Excel, Word, Outlook, Teams required.
- Experience with multi-center study protocols required.
- Bachelor's Degree Related Field of Study required
- Related post-bachelor's degree research experience 3-5 years 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 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
- Physician initiated (IDE or IND) trial experience preferred.
- Some direct experience working with the FDA on clinical trial audits is preferred.
- Graduate Diploma Related Field of Study 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
