The Vascular Care Group·Wellesley, Massachusetts
The role involves supporting clinical trial start-up activities and coordinating patient enrollment across multiple vascular care sites. Responsibilities include managing regulatory documents, entering data into CTMS and EDC systems, and ensuring compliance with IRB and FDA regulations.
Vascular Breakthroughs manages clinical trials for a growing group of vascular surgeons. Trials managed include device and drug trials. The trials range from being first in main pilot studies, IDE trials to post-market registry trials. We utilize a robust clinical trial management system that enables us to store all subject binders and regulatory binders electronically greatly facilitating remote management of trials and regulatory compliance.
This role is responsible for supporting clinical trials start-up activities and coordinating enrollment of patients across The Vascular Care Group (“TVCG”) in clinical trials.
Willingness to drive between TVCG sites to fulfill research requirements required; primary locations for work will be Wellesley, Plymouth, and Hyannis, with additional sites added as necessary. Role is comprised of 80% in person work, 20% remote.
A Bachelor's degree in biological, health, or social sciences is required, along with clinical experience in a surgical specialty. Knowledge of medical terminology and proficiency with computer systems for medical records are essential.
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.
