About the Role:
A growing clinical research team is seeking an experienced Clinical Research Coordinator II to
join their site operations in San Antonio. This position plays a key role in managing day-to-day
activities for assigned clinical trials, ensuring compliance with protocols, regulatory
requirements, and internal SOPs. This role will also involve working unblinded, overseeing
investigational product (IP) administration, and supporting junior team members.
You will work closely with monitors, sponsors, and site staff to ensure high-quality research
conduct and timely execution of study visits. Strong communication and organizational skills are
essential, along with a proactive, problem-solving mindset.
Key Responsibilities:
• Manage daily operations of clinical trials, including patient visits and regulatory
documentation
• Perform phlebotomy, vitals, EKGs, and oversee IP administration and accountability
• Serve as the lead coordinator on multiple studies, providing guidance and training to
junior staff
• Ensure adherence to protocol, GCP, and site SOPs
• Communicate effectively with sponsors, CROs, monitors, and investigators
• Maintain accurate records in the CTMS and study files
Qualifications:
• 2+ years of clinical research experience (required)
• Experience with phlebotomy, vitals, EKG (required)
• Previous oversight of IP management and unblinded procedures (required)
• Proven ability to lead multiple trials as a lead CRC (preferred)
• Strong written and verbal communication skills
• High-level medical terminology knowledge
• GED or high school diploma required; additional training preferred
• Spanish-speaking is a plus
Schedule:
Monday to Friday, 8:00 AM – 5:00 PM
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