Pediatrics Clinical Research Coordinator II

University of Texas Southwestern Medical Center; Dallas (TX); Presencial; USD 65.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

PPO medical plan

Paid Time Off

Retirement Programs

Paid Parental Leave

Tuition Reimbursement

Public Service Loan Forgiveness (PSLF)

Descripción de la vacante

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Coordinator II to support the Center for Inborn Errors of Immunity. You will coordinate patient recruitment, study visits, data collection, and regulatory tasks across translational studies.

Under PI supervision, you will handle IRB submissions, REDCap data management, and cross‑team collaboration; a CRC‑II role requiring strong organizational and regulatory skills, with certification within the first 6 months preferred.

Formación

• Bachelor’s degree in a medical or science related field.
• Minimum 2 years clinical research experience; advanced degree may substitute.
• Experience with IRB submissions and regulatory documentation.
• REDCap proficiency; knowledge of Epic and MS Office preferred.
• ACRP or SOCRA certification considered a plus.

Responsabilidades

• Coordinate patient recruitment, enrollment, and visit scheduling per protocol.
• Maintain IRB and regulatory documentation; prepare amendments as needed.
• Perform data collection, entry, validation, and basic analysis support.
• Support sample handling, biobanking, and study start‑up activities.
• Collaborate across departments and PI to ensure protocol compliance.

Conocimientos

Clinical research

IRB coordination

Data management

REDCap

Epic software

Microsoft Office

Statistical analysis

Educación

Bachelor's Degree in medical or science related field

Herramientas

REDCap

Epic

MS Office

R

Stata

SAS

GraphPad Prism

SPSS

Descripción del empleo

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Coordinator II to support the Center for Inborn Errors of Immunity. You will coordinate patient recruitment, study visits, data collection, and regulatory tasks across translational studies.

Under PI supervision, you will handle IRB submissions, REDCap data management, and cross‑team collaboration; a CRC‑II role requiring strong organizational and regulatory skills, with certification within the first 6 months preferred.