On-Site Clinical Research Coordinator — Temporary

Tekton Research; Austin (TX); On-site; USD 55,000 - 70,000; Full time

Job summary

Tekton Research in Austin, TX seeks a dedicated Clinical Research Coordinator (CRC) for a temporary on-site assignment to manage day-to-day study coordination, ensure GCP compliance, and liaise with investigators, sponsors and regulators.

The role involves coordinating multiple trials, recruiting and screening participants, collecting and shipping specimens, and maintaining source documents using EDC and CTMS to protect data integrity.

Qualifications

• Bachelor's degree in a relevant field preferred.
• 6 months to 1 year of CRC experience.
• Knowledge of GCP, FDA regulations and ICH guidelines.
• Experience with EDC systems and CTMS.
• Excellent communication and time-management skills.

Responsibilities

• Coordinate trials from start-up to close-out.
• Recruit, screen, consent and schedule participants per protocol.
• Collect, process, ship laboratory specimens per requirements.
• Maintain source documentation and regulatory binders per GCP/FDA.
• Monitor participant safety and report adverse events.
• Prepare IRB submissions, continuing reviews, and amendments.
• Collaborate with investigators, sponsors, monitors, and staff.
• Assist with monitoring visits and audits.
• Utilize EDC and CTMS to maintain study data.
• Ensure protocol compliance and research integrity.

Skills

GCP knowledge

FDA regulations

ICH guidelines

EDC systems

CTMS

MS Office

Time management

Communication

Education

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

Advanced degree preferred

Tools

EDC systems

CTMS

Microsoft Office

Job description

Tekton Research in Austin, TX seeks a dedicated Clinical Research Coordinator (CRC) for a temporary on-site assignment to manage day-to-day study coordination, ensure GCP compliance, and liaise with investigators, sponsors and regulators.

The role involves coordinating multiple trials, recruiting and screening participants, collecting and shipping specimens, and maintaining source documents using EDC and CTMS to protect data integrity.