Clinical Research Coordinator: Drive High-Impact Trials

Tekton Research; Wichita (KS); On-site; USD 52,000 - 68,000; Full time

Job summary

Tekton Research is a growth-oriented clinical research organization dedicated to conducting high-quality trials that advance patient care. The Clinical Research Coordinator (CRC) oversees day-to-day coordination, ensuring compliance with protocols and regulatory requirements while serving as a primary liaison among investigators, sponsors, participants, and regulators.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple trials in a

Qualifications

• Requires GCP, FDA regulations, ICH guidelines knowledge.
• Experience with pediatric and adult phlebotomy and specimen processing is preferred.
• Excellent organizational and time-management skills; ability to manage multiple studies

Responsibilities

• Coordinate and manage all aspects of assigned clinical trials from 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 high standards of participant care and research integrity.

Skills

GCP/FDA knowledge

EDC systems

Regulatory documentation

Microsoft Office

Communication skills

Multi-study management

Team collaboration

Education

High school diploma or GED

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

Tools

EDC systems

CTMS

Microsoft Office

Job description

Tekton Research is a growth-oriented clinical research organization dedicated to conducting high-quality trials that advance patient care. The Clinical Research Coordinator (CRC) oversees day-to-day coordination, ensuring compliance with protocols and regulatory requirements while serving as a primary liaison among investigators, sponsors, participants, and regulators.

This role requires excellent organizational skills, strong attention to detail, and the ability to manage multiple trials in a