Clinical Research Coordinator: Study Operations & IRB

Texas Tech University - Health Sciences Center; Amarillo (TX); On-site; USD 48,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Retirement plans

Wellness programs

Mother-friendly workplace

Job summary

TTUHSC in Amarillo, Texas is seeking a Clinical Research Coordinator to coordinate daily operations of clinical studies, oversee data management, and ensure compliance across assigned department(s). You will contribute to cultivating relationships with faculty and industry partners while supporting study quality and regulatory adherence.

Responsibilities include IRB submissions via Cayuse, training staff, and assisting with study budgets and documentation. Travel up to 15% may be required.

Qualifications

• Healthcare related training with current licensure/certification in their field
• Bachelor's degree from an accredited university with a major in the area of research being conducted
• Certification: CCRP or CCRC or ability to obtain certification within two years from date of hire or upon eligibility

Responsibilities

• Develop and maintain relationships with faculty members interested in or currently conducting clinical research.
• Develop and maintain relationships with pharmaceutical, medical device, and other manufacturers considering clinical trials.
• Facilitate IRB application and submission via Cayuse system.
• Recruit and enroll human subjects while protecting subjects' rights and ensuring compliance.

Education

Bachelor's degree in related field

Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) or eligible

Job description

TTUHSC in Amarillo, Texas is seeking a Clinical Research Coordinator to coordinate daily operations of clinical studies, oversee data management, and ensure compliance across assigned department(s). You will contribute to cultivating relationships with faculty and industry partners while supporting study quality and regulatory adherence.

Responsibilities include IRB submissions via Cayuse, training staff, and assisting with study budgets and documentation. Travel up to 15% may be required.