Job Description

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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