Clinical Trials Coordinator - Patient Care

UT MD Anderson; Houston (TX); On-site; USD 58,000 - 87,000; Full time

Benefits offered by this job

Medical coverage

Tuition assistance

Paid time off

Job summary

The University of Texas MD Anderson Cancer Center is seeking a Clinical Studies Coordinator to support patient care within clinical trials. The role involves coordinating protocol execution, maintaining regulatory compliance, and communicating with the study team to ensure patient safety.

Responsibilities include recruitment and follow-up of participants, documentation of adverse events, and collaboration with investigators and sponsors to uphold trial integrity.

Qualifications

• Requirements include a Bachelor's degree; Master’s preferred for advanced roles.
• Experience coordinating clinical trials and patient care is expected.
• Familiarity with IRB processes and regulatory documentation is important.

Responsibilities

• Coordinate and execute clinical trial activities in collaboration with PI and protocol team.
• Maintain up-to-date knowledge of protocol and regulatory requirements; ensure compliant data handling.
• Manage patient recruitment, scheduling, and follow-up in inpatient and outpatient settings.

Skills

Clinical trials coordination

Patient care

IRB/compliance

Communication skills

Education

Bachelor's degree

Master's degree in Public Health or related field

Tools

ePRTCL

CORe

Prometheus

ClinicalTrials.gov

Microsoft Office

Job description

The University of Texas MD Anderson Cancer Center is seeking a Clinical Studies Coordinator to support patient care within clinical trials. The role involves coordinating protocol execution, maintaining regulatory compliance, and communicating with the study team to ensure patient safety.

Responsibilities include recruitment and follow-up of participants, documentation of adverse events, and collaboration with investigators and sponsors to uphold trial integrity.