Clinical Research Coordinator II

Mass General Brigham•Boston, MA

1d•Onsite

About The Position

The Clinical Research Coordinator II will play a crucial role in supporting Phase 3 clinical trials focused on GLP-1 receptor agonists and an AI-assisted patient communication pilot study. These studies are pivotal in developing innovative treatment solutions for obesity management. The Phase 3 trial focuses on evaluating GLP-1 receptor agonists, while the pilot study investigates a bidirectional AI communication system designed to improve medication persistence, patient satisfaction, and provider workload through inbound support and scheduled outbound check-ins. This position involves collaboration with various departments to manage these clinical trials effectively, ensuring adherence to protocols and regulatory requirements.

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.

Nice To Haves

Can this role accept experience in lieu of a degree? Yes

Responsibilities

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.
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.
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.