Our client, a healthcare company operating a clinical research center in Boston, is hiring a Clinical Research Coordinator to manage day-to-day operations of ongoing patient studies. This role serves as the primary point of contact between study participants, principal investigators, and sponsors, ensuring that trials run in compliance with protocol and regulatory standards.
The coordinator will handle participant screening, consent processes, data collection, and study documentation. This position requires close attention to detail, strong organizational skills, and the ability to manage multiple studies simultaneously within a fast-paced clinical environment.
This is an on-site, full-time position based in Boston. The organization supports ongoing training and offers a clear path for coordinators interested in advancing into senior research or project management roles.
Responsibilities
Screen and enroll study participants according to protocol criteria
Obtain and document informed consent from participants
Schedule and coordinate participant visits and study procedures
Maintain accurate case report forms and source documentation
Track and report adverse events to principal investigators and sponsors
Ensure compliance with IRB, FDA, and GCP guidelines
Manage study supplies, lab kits, and specimen shipping logistics
Communicate with sponsors and monitors during site visits and audits
Requirements
Bachelor's degree in life sciences, nursing, or related field
2 or more years of clinical research or healthcare coordination experience
Working knowledge of GCP and IRB regulatory requirements
Strong written and verbal communication skills
Proficiency with electronic data capture systems
Ability to manage multiple studies and deadlines simultaneously
Experience with informed consent processes preferred