Clinical Research Assistant II — Data & Trials Coord

UT Southwestern Medical Center; Dallas (TX); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

PPO medical plan

Paid Time Off

TRS Retirement Programs

Paid Parental Leave

Wellness programs

Tuition Reimbursement

PSLF Qualified Employer

Job summary

UT Southwestern Medical Center is seeking a Clinical Research Assistant II to support ongoing data management for local and national studies. The role involves coordinating monitoring visits, preparing for audits, and interfacing with physicians and patients in cancer treatment trials.

Based in Richardson, this full-time position may require travel to regional clinics. Responsibilities include data submission, sample processing, eligibility review, consent, and coordinating trial activities

Qualifications

• Education as listed: high school diploma or associate's or bachelor’s degree in medical/science field.
• 2 years experience with high school diploma or 1 year experience with an associate’s degree.
• BLS/CPR/AED certifications may be required depending on affiliate location requirements.

Responsibilities

• Understands visit schedules, criteria and protocol requirements for low complexity trials (e.g., questionnaire, data registry, scripted); schedules research visits.
• Assists research staff by completing research protocol related tasks.
• Reviews and abstracts information from medical records including eligibility criteria.
• Enters data into case report forms or other data collection system based on research study.

Education

High School Diploma

Associate's Degree in medical or science related field

Bachelor's Degree medical or science related field

Tools

Data entry software

Job description

UT Southwestern Medical Center is seeking a Clinical Research Assistant II to support ongoing data management for local and national studies. The role involves coordinating monitoring visits, preparing for audits, and interfacing with physicians and patients in cancer treatment trials.

Based in Richardson, this full-time position may require travel to regional clinics. Responsibilities include data submission, sample processing, eligibility review, consent, and coordinating trial activities