Clinical Research Data Specialist II

UT Southwestern; Dallas (TX); Presencial; USD 55.000 - 75.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

PPO medical plan

Preventive care covered

Paid time off

Retirement benefits

Parental leave

Descripción de la vacante

UT Southwestern Medical Center in Dallas conducts clinical research studies and observational trials under investigator supervision. This role supports data management, documentation, and regulatory tasks across local and national studies, contributing to data integrity and study quality.

With required education and experience, the position involves coordinating visits, reviewing medical records, and assisting with sponsor audits and regulatory submissions as needed.

Formación

• Education: High School Diploma or Associate’s Degree in medical or science related field or Bachelor’s Degree in medical or science related field and no prior experience.
• Experience: 2 years experience with High School Diploma or 1 year experience with Associate’s Degree
• Preferred: Licenses/Certifications (BLS CPR) may be required based on affiliate location requirements.

Responsabilidades

• Understands visit schedules, criteria and protocol requirements for low complexity trials.
• Assists research staff by completing protocol related tasks.
• Reviews and abstracts information from medical records including eligibility criteria.
• Enters data into case report forms or data collection systems; maintains study documentation.

Conocimientos

Data management

Clinical research

QA/QC

IRB knowledge

Educación

High School Diploma or Associate's Degree in medical/science fields

Bachelor’s Degree in medical/science fields

Herramientas

Electronic data capture

Medical records review

Descripción del empleo

UT Southwestern Medical Center in Dallas conducts clinical research studies and observational trials under investigator supervision. This role supports data management, documentation, and regulatory tasks across local and national studies, contributing to data integrity and study quality.

With required education and experience, the position involves coordinating visits, reviewing medical records, and assisting with sponsor audits and regulatory submissions as needed.