Peregrine Team·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.
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.
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.
Market context
Clinical Research Coordinator roles in Massachusetts often draw candidates with both patient-facing clinical experience and research coordination skills, especially in academic medical centers, hospitals, and study sites. Competition can be stronger for applicants who can show familiarity with basic clinical procedures, strong computer skills, and the required credential or degree mix. Review the AI-summarized requirements and benefits here to quickly compare fit before applying, then tailor your resume to highlight research, documentation, and patient interaction experience.
