Clinical Research Coordinator I — Launch Your Trials Career

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance day one

100% preventive care coverage

Paid Time Off from day one

Retirement Program

Paid Parental Leave

Tuition Reimbursement

PSLF Qualified Employer

Job summary

UT Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator to support Investigator-led studies through patient coordination, data collection, and regulatory compliance. The role emphasizes meticulous data quality, participant safety, and collaboration across research teams in a fast-paced environment within a leading academic medical center.

Experience in clinical research and knowledge of regulatory standards are preferred, with opportunities for professional growth and

Qualifications

• Bachelor's degree or higher in medical or science field.
• Minimum 1 year of clinical research experience.
• Bilingual English/Spanish preferred.

Responsibilities

• Interacts with clinical research participants by phone, telehealth, or in person.
• Coordinate regulatory activities to ensure FDA and university policy compliance.
• Schedule study procedures according to protocol and assist PI as needed.
• Screen, recruit, enroll and follow subjects per protocol.
• Maintain data collection, develop CRFs, and support data entry.
• Assist in developing and implementing research studies, including protocol writing.
• Monitor safety and ensure HRPP-compliant reporting.

Skills

Clinical research coordination

Regulatory compliance

Data management

Budget management

Contract administration

Bilingual English/Spanish

Education

Bachelor's degree in medical or science field

Tools

Clinical trial management system

Electronic Medical Records (EMR)

Data entry systems

Job description

UT Southwestern Medical Center in Dallas seeks a Clinical Research Coordinator to support Investigator-led studies through patient coordination, data collection, and regulatory compliance. The role emphasizes meticulous data quality, participant safety, and collaboration across research teams in a fast-paced environment within a leading academic medical center.

Experience in clinical research and knowledge of regulatory standards are preferred, with opportunities for professional growth and