Clinical Research Data Specialist II - Trials & Impact

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 48,000 - 62,000; Full time

Benefits offered by this job

PPO medical plan

Paid Time Off

Tuition Reimbursement

Paid Parental Leave

Job summary

University of Texas Southwestern Medical Center seeks a Clinical Research Assistant II at Simmons Cancer Center. The role focuses on centralized data management for local and national studies, ensuring timely and accurate data entry, QA/QC, and regulatory readiness.

Collaboration with study teams supports data quality and compliance. The position involves assisting with consent, recruitment, and preparation of study records for audits, under supervision of investigators and coordinators.

Qualifications

• Education requirements include High School Diploma, or an Associate's/Bachelor's in medical/science fields.
• Experience requirements: 2 years with HS, 1 year with Associate.
• Licenses/certifications (CPR/CPR AED/BLS) may be required depending on affiliate location.

Responsibilities

• Enters data into case report forms or data collection systems and aids with study documentation.
• Reviews medical records to determine eligibility and supports protocol adherence.
• Assists with data queries, QA/QC checks, and regulatory submissions as needed.
• Recruits and enrolls patients under supervision and assists with consent planning and documentation.
• Prepares for sponsor/audit activities and maintains data integrity across databases.

Skills

Data management

Data entry

Regulatory compliance

Clinical research

QA/QC

Recruitment

Consent/IRB

Education

High School Diploma

Associate's Degree in medical or science related field

Bachelor's Degree in medical or science related field

Job description

University of Texas Southwestern Medical Center seeks a Clinical Research Assistant II at Simmons Cancer Center. The role focuses on centralized data management for local and national studies, ensuring timely and accurate data entry, QA/QC, and regulatory readiness.

Collaboration with study teams supports data quality and compliance. The position involves assisting with consent, recruitment, and preparation of study records for audits, under supervision of investigators and coordinators.