About this role

Conduct and coordinate all aspects of clinical trial activities at the site.
Perform phlebotomy on patients, following proper clinical and safety protocols.
Recruit, screen, and enroll study participants according to inclusion/exclusion criteria.
Schedule and conduct study visits, ensuring adherence to protocol requirements.
Accurately collect, process, and ship biological samples per study-specific guidelines.
Complete and maintain study documentation, including source documents, regulatory binders, and informed consent forms.
Perform timely and accurate data entry into electronic data capture systems (EDC).
Communicate effectively with sponsors, monitors, and other research team members.
Ensure compliance with GCP, ICH, FDA, and IRB regulations.
Assist in monitoring visits and audit preparation as needed.

Minimum of 1–2 years of experience as a Clinical Research Coordinator, in a similar environment.
Phlebotomy certification or demonstrated competency in venipuncture (pediatric and adult required).
Strong understanding of clinical trial operations, regulatory documentation, and data management.
Excellent attention to detail, organization, and time management skills.
Strong interpersonal and communication abilities with patients and clinical staff.
Proficient in Microsoft Office and electronic data capture systems.
CPR certification preferred.

Clinical Research Coordinator, CRC

Key skills