Senior Clinical Research Coordinator - Global Health

Mass General Brigham•Boston, MA

7d•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, and offers opportunities to contribute to broader public health and health policy research initiatives. Applicants must upload a cover letter specific to the role in the Center and a resume. Applications missing either component will not be considered.

Requirements

Bachelor's degree in a related field required, or a graduate diploma in a related field preferred; experience may be accepted in lieu of a degree.
Related post-bachelor's degree experience 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 display initiative in introducing innovations to research studies.
Excellent time management, organizational, interpersonal, written, and verbal communication skills.

Nice To Haves

Graduate diploma in a related field.

Responsibilities

Recruit, engage, consent, and support study participants.
Assist with the design and implementation of study materials and operational plans.
Maintain study databases, including 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.