On-Site Clinical Research Coordinator: Drive Trials

ADP, Inc.; Oklahoma City (OK); On-site; USD 48,000 - 60,000; Full time

Job summary

Tekton Research in Oklahoma City is seeking a Clinical Research Coordinator to manage day-to-day coordination of clinical trials. The CRC will serve as primary liaison among investigators, sponsors, participants, and regulators, ensuring data integrity and participant safety.

This on-site role requires meticulous organization and the ability to manage multiple studies in a fast-paced environment. The ideal candidate has a high school diploma or GED (Bachelor’s preferred) and 6–12 months of CRC

Qualifications

• Required: High school diploma or GED; Bachelor's degree preferred.
• Minimum 6–12 months of Clinical Research Coordinator experience.
• GCP, FDA regulations, ICH guidelines knowledge.
• Experience with pediatric and adult phlebotomy and specimen processing.
• Strong organizational and time management with multitasking ability.
• Proficiency with EDC systems and MS Office.
• Excellent verbal and written communication skills.

Responsibilities

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

Skills

Excellent communication

Organizational skills

Time management

Independent work

Team collaboration

Phlebotomy experience

Education

Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or related field

Advanced degree in Nursing, Public Health, Clinical Research, or related field

Tools

EDC systems

Microsoft Office

Job description

Tekton Research in Oklahoma City is seeking a Clinical Research Coordinator to manage day-to-day coordination of clinical trials. The CRC will serve as primary liaison among investigators, sponsors, participants, and regulators, ensuring data integrity and participant safety.

This on-site role requires meticulous organization and the ability to manage multiple studies in a fast-paced environment. The ideal candidate has a high school diploma or GED (Bachelor’s preferred) and 6–12 months of CRC