Clinical Research Job at UT Southwestern Medical Center | Apply Now
If you are looking for a clinical research job in a leading academic medical center, UT Southwestern Medical Center is hiring a Clinical Research Coordinator I at Simmons Cancer Center in Fort Worth. This opportunity is ideal for candidates with clinical research experience who want to grow in oncology trials and patient-centered research. Among top medical jobs in Texas, this role offers career growth, strong benefits, and the chance to work at a nationally ranked institution.
Job Details:
- Job Position: Clinical Research Coordinator I
- Job ID: 926287
- Department: Simmons Cancer Center – Clinical Research Office
- Location: Fort Worth, Texas
About the Company:
UT Southwestern Medical Center is a world-renowned academic medical and research institution with over 75 years of excellence in Dallas-Fort Worth, Texas. Ranked as the number 1 hospital in Dallas-Fort Worth by U.S. News & World Report, the institution is known for innovation, teamwork, and compassionate patient care. For professionals seeking stable and growth-focused medical jobs, this organization provides long-term career development opportunities.
Job Description:
This clinical research job involves managing patient activity on clinical oncology trials for Simmons Cancer Center regional clinics. The Clinical Research Coordinator I will divide time between two Fort Worth clinics and the Clearfork clinic, with potential travel to other regional clinics as needed. This opportunity stands out among medical jobs in oncology research due to its direct patient interaction and involvement in advanced clinical trials.
Qualifications:
Required Education: Bachelor’s Degree or higher in a medical field
Required Experience:
- Minimum 1 year of clinical research experience
- Additional years of experience or advanced degrees may substitute for education or experience requirements.
Preferred Certifications:
- BLS (Basic Life Support), if required by study protocol
- CPR AED Licensure, if required
- ACRP or SOCRA certification preferred
Key Responsibilities:
- Direct interaction with clinical research participants via telephone, telehealth, or in person
- Coordinate regulatory aspects of clinical trials in compliance with FDA requirements, University policies, and hospital standards
- Schedule and coordinate study procedures according to approved protocols
- Screen, recruit, enroll, and follow research participants
- Assist with the consent process
- Maintain and coordinate study data collection, including CRFs and data tools
- Assist in writing clinical research protocols
- Conduct study procedures with proper training and scope of work compliance
- Assist with research budgets and billing activities
- Review and abstract medical records for trial eligibility verification
- Monitor patient safety and ensure proper reporting
- Review the study’s feasibility
- Assist in marketing and recruitment through website or social media efforts
- Develop proficiency in clinical trial management systems and electronic medical records
- Maintain subject-level documentation
- Perform additional duties as assigned
