Clinical Research Coordinator
The Clinical Research Coordinator manages day-to-day clinical trial activities at the site level, ensuring studies are conducted according to protocol, GCP, and regulatory requirements while supporting patient safety and data integrity.
Responsibilities:
Coordinate participant recruitment, screening, enrollment, and follow-up
Collect and document study data in compliance with protocols
Assist investigators with study visits and procedures
Manage regulatory documents and maintain study records
Serve as primary liaison between the site, sponsor, and CRO
Skills & Experience:
Bachelor’s degree in life sciences, nursing, or related field
Experience in clinical research or monitoring preferred
Knowledge of GCP and FDA regulations
Strong organizational and communication skills
EEO Employer
We are an equal opportunity employer and comply with all applicable federal, state, and local fair employment practices laws. We strictly prohibit and do not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, sexual orientation, gender (including gender identity and expression), marital or familial status, age, physical or mental disability, perceived disability, citizenship status, service in the uniformed services, genetic information, or any other characteristic protected under applicable federal, state, or local law. Applications from members of minority groups and women are encouraged.