Clinical Research Coordinator

Lange Recruiting•Richmond, VA

4d•Onsite

About The Position

Tekton Research is seeking a motivated, detail-oriented Clinical Research Coordinator to manage clinical research studies in Richmond, Virginia. The position works primarily with an established private endocrinology practice, with additional research involvement at a local pediatric practice. The coordinator has dedicated office space within the medical practice and works closely with physicians, study participants, research sponsors, and research teams to coordinate clinical trials and support high-quality patient care. The role coordinates studies from initiation through completion, including participant recruitment and study procedures, documentation and regulatory compliance, and coordination with laboratories and sponsors. Clinical research experience is required; pediatric phlebotomy experience is preferred but not required.

Requirements

Prior Clinical Research Coordinator experience, with a minimum of 1 year.
Experience coordinating clinical trials and maintaining regulatory documentation.
Knowledge of GCP guidelines, FDA regulations, and clinical research procedures.
Strong organizational, communication, and problem-solving skills.
Ability to work independently, manage multiple priorities, and collaborate effectively with physicians and research teams.
Experience with electronic data capture (EDC) systems.

Nice To Haves

2 or more years of Clinical Research Coordinator experience.
Pediatric phlebotomy experience.
Bachelor's degree in a healthcare or science-related field.

Responsibilities

Coordinate and manage clinical research studies from initiation through completion.
Recruit, screen, consent, and schedule study participants.
Collaborate with physicians, sponsors, and research teams to ensure successful study execution.
Maintain accurate study documentation, regulatory records, and electronic data capture (EDC) systems.
Perform study-related procedures, including vital signs, ECGs, and specimen collection, as appropriate.
Coordinate laboratory specimen collection, processing, and shipment.
Monitor participant safety and ensure compliance with study protocols, Good Clinical Practice (GCP), and FDA regulations.
Assist with sponsor monitoring visits, audits, and regulatory inspections.