Clinical Research Coordinator

Responsibilities:

Assist with clinical trial regulatory document management Prepare and maintain electronic regulatory binders Enter and review study data in Electronic Data Capture (EDC) systems Track study documentation and investigator training records Support subject recruitment and pre-screening activities Assist with adverse event and protocol deviation documentation Review medical records and source documents for completeness Prepare reports, logs, trackers, and study-related correspondence Schedule investigator meetings and training sessions Support quality assurance and compliance activities Coordinate with investigators, sponsors, and CROs globally

Requirements:

Bachelor's degree or higher in: Medicine, Nursing, Pharmacy, Medical Laboratory Science, Public Health, Biological Sciences, and Life Sciences or related field Excellent written and spoken English Strong computer skills and proficiency with Microsoft Office Reliable internet connection and personal computer Close attention to detail and ability to meet deadlines Ability to work during U.S. business hours

Preferred Qualifications:

Prior clinical research experience GCP certification Experience with EDC systems Experience with regulatory documentation Healthcare or medical records experience

Benefits:

Comprehensive clinical research training Exposure to global clinical trial operations Career development opportunities Mentorship from experienced investigators and research professionals Competitive compensation Long-term growth potential within a rapidly expanding research organization