Clinical Research Coordinator II

Mass General Brigham • Boston, MA

9d • $24 - $35 • Onsite

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. The CRC II will work under the direction of the Clinical Research Manager to coordinate all aspects of industry-sponsored and physician-sponsored research studies, including subject recruitment, data collection, scheduling of study-related activities, and follow-up of enrolled subjects. The CRC II will collaborate with multiple departments, sponsors, and monitors to ensure productivity and timely completion of studies. S/he will provide guidance and direction to clinical investigators, research personnel, and subjects. The CRC II will ensure compliance with study protocols, regulations, and ethical standards in accordance with federal law/regulations (HIPAA/CFR), institutional policies and Good Clinical Practice guidelines. The CRC II will be a resource for teaching other personnel about the research processes, protocols, and databases.

Requirements

• At least 1 year experience coordinating clinical research protocols with human subjects and IRB submissions.
• Computer proficiency in MS Excel, Word, Outlook, Teams required.
• Bachelor's Degree Science required
• Related post-bachelor's degree research experience 1-2 years required
• Ability to work more independently and as a team member.
• Computer literacy, analytical skills, and ability to resolve technical problems.
• Ability to interpret the acceptability of data results.
• Working knowledge of data management programs.

Nice To Haves

• Professional certification in clinical research preferred.

Responsibilities

• Assists with determining the suitability of study subjects and acts as a resource for patients and families.
• Has input into recruitment strategies and may contribute to protocol recommendations.
• Administers scores and evaluates study questionnaires.
• Maintains research data, patient files, regulatory binders, and study databases.
• Performs data analysis and QA/QC checks and organizes and interprets data.
• Assists with preparation for annual review and assists PI in completing study reports and presentations.
• May assist with training and orientation of new staff members.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level