Clinical Research Coordinator | Drive Impactful Trials

Tekton Research; Oklahoma City (OK); On-site; USD 45,000 - 65,000; Full time

Job summary

Tekton Research is seeking a Clinical Research Coordinator (CRC) to oversee day-to-day coordination of clinical studies in a fast-paced environment. You will ensure adherence to study protocols, GCP, and regulatory requirements while serving as the primary liaison among investigators, sponsors, study participants, and regulatory bodies.

Ideal candidates bring a bachelor's degree in a related field, 6–12 months of CRC experience, strong organizational skills, and proficiency with EDC systems and

Qualifications

• High school diploma or GED required; Bachelor's degree in Nursing, Biology, Health Sciences, Public Health, or a related field preferred.
• Minimum of six months to one year of Clinical Research Coordinator experience.
• Working knowledge of GCP, FDA regulations, ICH guidelines, and clinical research processes.
• Experience with pediatric and adult phlebotomy and specimen processing.
• Strong organizational and time management skills with the ability to prioritize multiple studies.
• Experience maintaining regulatory documentation and source records.
• Proficiency with EDC systems and Microsoft Office applications.
• Excellent verbal and written communication skills.
• Ability to work independently while collaborating effectively with multidisciplinary teams.

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

Organization

Team collaboration

Attention to detail

Education

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

Advanced degree in Nursing or Public Health

Tools

EDC systems

Microsoft Office

Job description

Tekton Research is seeking a Clinical Research Coordinator (CRC) to oversee day-to-day coordination of clinical studies in a fast-paced environment. You will ensure adherence to study protocols, GCP, and regulatory requirements while serving as the primary liaison among investigators, sponsors, study participants, and regulatory bodies.

Ideal candidates bring a bachelor's degree in a related field, 6–12 months of CRC experience, strong organizational skills, and proficiency with EDC systems and