Clinical Research Coordinator – San Antonio, Texas Rapidly Clinical Research Organisation

A leading and rapidly growing clinical research organisation is seeking an experienced Clinical Research Coordinator (CRC) to join its San Antonio research team.

This is an excellent opportunity for a hands-on CRC who enjoys a fast-paced, participant-facing research environment and wants to work across a diverse portfolio of clinical trials.

As a Clinical Research Coordinator, you will be responsible for the day-to-day coordination and execution of clinical trials, working closely with participants, Principal Investigators, sponsors, and the wider research team.

You will play a key role in ensuring studies are delivered safely, efficiently, and in accordance with protocol, GCP, and applicable regulatory requirements.

• Coordinate clinical trials from start-up through close-out
• Conduct participant visits and ensure protocol-required procedures are completed
• Perform or assist with vital signs, 12-lead ECGs, phlebotomy, specimen collection and processing
• Complete informed consent and participant screening activities
• Review medical histories and assess participant eligibility against protocol criteria
• Maintain accurate source documentation and study records
• Enter and maintain clinical data within EDC systems
• Manage investigational product accountability where required
• Coordinate laboratory samples, shipments and processing
• Support recruitment, screening and participant retention activities
• Communicate effectively with Principal Investigators, sponsors, monitors and vendors
• Respond to data queries and support monitoring visits
• Ensure all study activities remain compliant with ICH-GCP, FDA regulations, protocol requirements and SOPs
• Assist with regulatory documentation, essential documents and study files
• Support audits, inspections and study close-out activities

• Previous experience as a Clinical Research Coordinator within a clinical research site environment
• Experience working directly with clinical trial participants
• Strong understanding of ICH-GCP and clinical research regulations
• Hands-on experience with clinical trial procedures
• Phlebotomy, ECG and vital signs experience strongly preferred
• Experience with electronic data capture (EDC) systems
• Strong attention to detail and documentation skills
• Ability to manage multiple studies and competing priorities
• Excellent communication and interpersonal skills
• Comfortable working in a fast-paced, high-volume research environment
• Ability to work effectively with investigators, sponsors and cross-functional teams

• Join a growing clinical research organisation
• Exposure to a diverse and expanding clinical trial portfolio
• Hands-on involvement across the full clinical trial lifecycle
• Opportunity to develop within a high-performing research environment
• Work alongside experienced investigators and clinical research professionals
• Strong opportunity for career progression and internal growth