POSITION SUMMARY:

Our Clinical Research Coordinators (CRCs) are central to our mission of advancing science while delivering patient-centered care. Guided by our ICROP values — Integrity, Commitment to Accountability, Relentless Improvements, Ownership Mindset, and Patient-Centeredness — the CRC manages study operations, ensures compliance, supports participants, and maintains the highest quality standards in clinical research.

QUALIFICATIONS:

• Bachelor’s degree required (life sciences, nursing, or related field).
• At least 1 year of research coordination experience is required.
• Any clinical experience related to vital signs, ECG, phlebotomy, medical history, and medical terminology is a plus.
• Demonstrated ability to provide patient/participant centered care.
• Certification (CCRC or equivalent) preferred but not required; training opportunities available.
• Proficiency with Microsoft Office Suite, Outlook, and database systems required.
• Experience with EDC, IWRS/IRT, ePRO, CTMS, and eSource platforms preferred.
• Familiarity with ICH-GCP E6(R2), HIPAA, safety monitoring, and human subject protections.
• Must be comfortable working in-person in Beaumont, TX.

BRING HOPE TO PATIENTS. BUILD A CAREER WITH PURPOSE.

Gadolin Research is a clinical research site in Beaumont, TX. We are professional, innovative, customer-centric and our goal is to improve the quality of life and health of our patients. We conduct clinical research studies that help make groundbreaking medicine accessible so that people everywhere can benefit.

REGULATORY & ACCOUNTABILITY

• Work with the regulatory coordinator to prepare and submit IRB applications and amendments.
• Act as the day-to-day liaison with the IRB and Human Research Committee.
• Ensure consistency and compliance across all regulatory documents.
• Participate in protocol operations manual development and adherence.