Clinical Research Coordinator: Fast-Paced On-Site Trials

Tekton Research Inc; San Antonio (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Tekton Research is seeking a Clinical Research Coordinator to manage day-to-day coordination of clinical trials on-site in San Antonio, ensuring protocol, GCP, and regulatory compliance. You will act as the primary liaison among investigators, sponsors, participants, and regulatory bodies, safeguarding participant safety and data integrity.

The ideal candidate has a high school diploma or GED with 6–12 months CRC experience or a bachelor's degree in a related field, strong organizational and

Qualifications

• High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out.
• Recruit, screen, consent, and schedule study participants according to protocol requirements.
• Collect, process, package, and ship laboratory specimens according to protocol and sponsor requirements.
• Maintain accurate source documentation, regulatory binders, and study records in compliance with GCP, FDA regulations, and institutional policies.
• Monitor participant safety and promptly identify, document, and report adverse events.
• Prepare and submit regulatory documents, including IRB submissions, continuing reviews, and protocol amendments.
• Collaborate with investigators, sponsors, monitors, and study staff to ensure successful study conduct.
• Assist with monitoring visits, sponsor audits, and regulatory inspections.
• Utilize EDC systems and CTMS to maintain accurate study data.
• Ensure protocol compliance while maintaining the highest standards of participant care and research integrity.

Skills

Communication

Organizational skills

Time management

Team collaboration

Independent work

GCP knowledge

EDC systems

MS Office

Education

High school diploma

Bachelor's degree in Nursing

Bachelor's degree in Biology

Bachelor's degree in Public Health

Bachelor's degree in Health Sciences

Tools

EDC systems

CTMS

Microsoft Office

Job description

Tekton Research is seeking a Clinical Research Coordinator to manage day-to-day coordination of clinical trials on-site in San Antonio, ensuring protocol, GCP, and regulatory compliance. You will act as the primary liaison among investigators, sponsors, participants, and regulatory bodies, safeguarding participant safety and data integrity.

The ideal candidate has a high school diploma or GED with 6–12 months CRC experience or a bachelor's degree in a related field, strong organizational and