Mass General Brigham · 1 hour ago
Clinical Research Coordinator 1
Mass General Brigham is a not-for-profit organization that supports patient care, research, teaching, and community service. The Clinical Research Coordinator 1 will assist in clinical research studies, including recruiting and evaluating patients, collecting and organizing data, and performing clinical tests. This role involves coordinating multi-center trials and ensuring compliance with regulatory standards.
Health CareHome Health CareMedical
Responsibilities
Provide support to the Principal Investigator (PI, Aleksandar Videnovic, MD MSc), co-investigators, and all other study collaborators
Ensure regulatory requirements are met in accordance with GCP (Good Clinical Practice) and HIPAA (Protection of Human Research Subjects) standards
Assist in the maintenance of all study regulatory documents, including the preparation of annual IRB submissions, any needed IRB modifications, correspondence with the study sponsors, and the physical regulatory binder
Verify accuracy of study forms
Regularly inform PI and study team of progress towards recruitment targets and milestones
Assist the Principal Investigator in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials
Perform other related duties as required (e.g., data entry, data checking/cleaning, literature reviews)
Prepare data for analysis and data entry
Work with PI to prepare and complete study reports
Provide a basic explanation of study details and, in some cases, obtain informed consent from subjects
Assist in the administration of clinical assessments of the study subjects, including but not limited to screening, evaluation, and administration of online assessments to participants, and coordination of biospecimen collection
Assist with the setup of sleep studies, actigraphy, and pupillometry
Communicate frequently with MGH employees and sponsor representatives to ensure study visits are conducted appropriately
Abstract medical records
Contact participants regarding scheduling and data collection
Assist with data collection, processing, entry, storage, and quality control for clinical research studies
Coordinate study intervention sessions
Participate in subject recruitment and assist with determining the suitability of research subjects
Assist with developing and implementing recruitment strategies
Complete study visits that require EKG, phlebotomy, and vital signs collection
Qualification
Required
Bachelor's Degree Related Field of Study required
Ability to work well independently as well as with co-workers, peers, supervisors, and patients
Careful attention to detail and accuracy
Ability to manage multiple tasks & priorities, and set deadlines
Computer literacy
Working knowledge of clinical research protocols
Analytical skills and ability to resolve technical problems
Excellent communication and interpersonal skills
Strong organizational and data management skills
Preferred
Some relevant research project work 0-1 year preferred
Benefits
Comprehensive benefits
Career advancement opportunities
Differentials
Premiums
Bonuses
Company
Mass General Brigham
Mass General Brigham specializes in providing medical treatments and health diagnostics services.
H1B Sponsorship
Mass General Brigham has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (77)
2024 (61)
2023 (93)
2022 (70)
2021 (80)
2020 (29)
Funding
Current Stage
Late StageLeadership Team
Recent News
Research & Development World
2026-01-25
Longevity.Technology
2026-01-24
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