Clinical Research Coordinator I - Entry-Level Research

University of Texas Southwestern Medical Center; Dallas (TX); Vor Ort; USD 52.000 - 76.000; Vollzeit

Benefits dieser Stelle

PPO medical plan

100% preventive care

Paid Time Off

TRS retirement

Parental Leave

Wellness programs

Tuition Reimbursement

PSLF

Zusammenfassung

UT Southwestern Medical Center in Dallas is seeking a Clinical Research Coordinator to support patient and participant coordination, data management, and regulatory compliance across multiple studies led by Dr. Woods and Dr. Gimpel.

The role includes study conduct, data collection, reporting, and collaboration with investigators and students in community health projects. Responsibilities span participant screening, enrollment, IRB documentation, and dissemination of findings, with emphasis on

Qualifikationen

• Bachelor's Degree or higher in medical or science related field.
• 1 year of clinical research experience. Additional experience or advanced degree may substitute.
• Licenses/certifications such as CPR/BLS; CPR AED a plus (preferred).

Aufgaben

• Coordinate regulatory aspects of trials to comply with policies and FDA requirements.
• Screen, recruit, enroll and follow subjects per protocol; assist with consent when needed.
• Develop data collection tools and CRFs; maintain study documentation.
• Prepare and submit IRB materials; ensure PHI protection and regulatory compliance.
• Lead and support dissemination of findings through reports, presentations, and manuscripts.
• Maintain data quality and integrity across the study lifecycle.

Kenntnisse

Clinical research terminology

Computer skills

Communication skills

PHI compliance

Confidential data handling

Problem solving

Ausbildung

Bachelor's Degree or higher in medical/science field

Jobbeschreibung

UT Southwestern Medical Center in Dallas is seeking a Clinical Research Coordinator to support patient and participant coordination, data management, and regulatory compliance across multiple studies led by Dr. Woods and Dr. Gimpel.

The role includes study conduct, data collection, reporting, and collaboration with investigators and students in community health projects. Responsibilities span participant screening, enrollment, IRB documentation, and dissemination of findings, with emphasis on