On-Site Clinical Research Coordinator — Temporary Role

ADP, Inc.; Beaumont (TX); On-site; USD 52,000 - 76,000; Part time

Job summary

Tekton Research in Beaumont, TX is seeking a Clinical Research Coordinator for a temporary, on-site role. You will oversee day-to-day coordination of clinical studies, ensuring protocol adherence, GCP compliance, and data integrity while serving as the liaison between investigators, sponsors, and participants.

The CRC will recruit and screen participants, manage specimens and regulatory documents, and support audits and inspections in a fast-paced research setting.

Qualifications

• High school diploma or GED required; Bachelor's degree preferred in Nursing, Biology, Health Sciences, or Public Health.
• 6–12 months of Clinical Research Coordinator experience.
• Knowledge of GCP, FDA regulations, and ICH guidelines.
• Experience with pediatric and adult phlebotomy and specimen processing.
• Proficiency with Electronic Data Capture (EDC) systems and MS Office.

Responsibilities

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

Skills

Regulatory compliance

GCP knowledge

IRB submissions

EDC systems

Time management

Communication skills

Independent worker

Education

Bachelor’s degree (Nursing/Biology/Health Sci)

Advanced degree in Nursing/Public Health/Clinical Research

Tools

Microsoft Office

Job description

Tekton Research in Beaumont, TX is seeking a Clinical Research Coordinator for a temporary, on-site role. You will oversee day-to-day coordination of clinical studies, ensuring protocol adherence, GCP compliance, and data integrity while serving as the liaison between investigators, sponsors, and participants.

The CRC will recruit and screen participants, manage specimens and regulatory documents, and support audits and inspections in a fast-paced research setting.