Peregrine Team
Location
Boston, Massachusetts
The Clinical Research Coordinator will manage daily clinical trial activities, including patient scheduling and regulatory compliance. They will also serve as a key liaison between investigators, sponsors, and patients while ensuring accurate data entry into EDC systems.
Candidates must hold a Bachelor’s degree in Life Sciences or a related field. Additionally, 2–4 years of clinical research experience and a strong understanding of GCP and clinical trial processes are required.
Peregrine Team is seeking a Clinical Research Coordinator to support clinical trial operations for a leading pharmaceutical organization. This individual will play a critical role in ensuring studies are executed efficiently, ethically, and in compliance with regulatory standards. Key Responsibilities Coordinate day-to-day clinical trial activities, including patient scheduling and follow-ups Maintain regulatory binders and ensure compliance with GCP and IRB requirements Assist with study start-up, monitoring visits, and close-out activities Collect and enter clinical data accurately into EDC systems Serve as a liaison between investigators, sponsors, and patients
Bachelor’s degree in Life Sciences or related field 2–4+ years of clinical research experience Strong knowledge of GCP and clinical trial processes Excellent organizational and interpersonal skills
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