Senior Clinical Research Coordinator - Global Health

Mass General Brigham•Boston, MA

8d•$82,014•Onsite

About The Position

The Senior Clinical Research Coordinator position at the Medical Practice Evaluation Center (MPEC) within Massachusetts General Hospital supports investigator-led clinical research studies focused primarily on upper respiratory infections. The role coordinates and implements multi-year household research studies, engages participants, manages study operations and logistics, ensures data quality and regulatory compliance, and collaborates with internal and external partners to achieve research goals. The position requires project management, communication, clinical research, and data management skills, with opportunities to contribute to broader public health and health policy research initiatives. Patient care is not required. Applicants must upload a cover letter specific to the role and Center and a resume; applications without both will not be considered.

Requirements

Bachelor's degree in a related field required, or related graduate diploma preferred; the role can accept experience in lieu of a degree.
Related post-bachelor's degree required.
Three to five years of research experience required.
Ability to work independently and as a team member.
High degree of computer literacy and analytical skills.
Ability to identify 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.
Ability to show initiative in introducing innovations to research studies.
Excellent time management, organizational, interpersonal, written, and verbal communication skills.

Responsibilities

Recruit, engage, consent, and support study participants.
Assist with the design and implementation of study materials and operational plans.
Maintain study databases (REDCap), enter data, and perform quality assurance checks.
Coordinate day-to-day study activities, schedules, enrollment goals, and reporting requirements.
Serve as a liaison among participants, laboratories, sponsors, courier services, and clinical staff.
Track project timelines, milestones, deliverables, and progress reports.
Assist with staff onboarding and training when needed.
Procure and manage study supplies and inventory.
Maintain compliance with human-subjects research regulations and study protocols.
Communicate study procedures, protocols, and data requirements to stakeholders.
Build productive relationships with internal and external research partners.