Clinical Research Coordinator II

Mass General Brigham • Boston, MA

1d • $24 - $39 • Hybrid

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 MGH Neuroendocrine Unit is looking for an enthusiastic candidate for a per diem clinical research coordinator position to work on projects related to female athletes and hormonal health. The candidate will work with a dynamic team of physicians, nurse practitioners, and other clinical research coordinators. The prospective study coordinator will be supervised by the study clinician team and responsible for various aspects of clinical trial management and administrative tasks, including but not limited to scheduling and carrying out study visits, clinical trial protocol management, subject recruitment, data entry, and regulatory management. Projects mainly focus on the intersection between endocrinology and sports medicine in female athletes, including metabolic bone health, relative energy deficiency in sport (REDs), and menstrual cycle and athletic performance. 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, it provides input into determining study subject suitability and input into recruitment strategy. Performs data analysis, interpretation, QA/QC, and assists in completing reports and presentations.

Requirements

• 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.

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

• Career Level: Mid Level