Clinical Research Assistant II — Data & Trials Specialist

University of Texas Southwestern Medical Center; Dallas (TX); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

PPO medical plan

Paid Time Off

Retirement Programs through TRS

Paid Parental Leave

Tuition Reimbursement

PSLF Qualified Employer

Wellness programs

Job summary

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Assistant II to support data management for local and national studies. The role may involve coordinating observational trials, consenting participants, and assisting with study documentation under PI guidance.

Based at Richardson, the position may travel to regional clinics for coverage needs, contributing to monitor visits, data submission, and coordination of trial activities through the continuum of care.

Qualifications

• Knowledge of applicable Federal and institutional regulations governing clinical research.
• Knowledge of clinical research protocols.
• Effective organizational skills and attention to detail.
• Proactively works to maximize results of the team and organization.
• Follows and understands the regulations for Protected Health Information (PHI).
• Possess strong computer skills (spreadsheets, databases, and interactive web-based software).
• Possess good communication skills.

Responsibilities

• Interact with investigators, staff and participants to coordinate trial activities.
• Enter and verify data in case report forms and data systems.
• Schedule visits and monitor study progress and audits.
• Ensure data quality and regulatory compliance for regulatory submissions.
• Assist with preparing reports and IRB submissions and audits.
• Support recruitment and enrollment of participants when needed.

Skills

Organizational skills

Computer skills

Communication skills

PHI regulations

Problem solving

Education

High School Diploma

Associate's Degree

Bachelor's Degree

Job description

UT Southwestern Medical Center in Dallas, TX seeks a Clinical Research Assistant II to support data management for local and national studies. The role may involve coordinating observational trials, consenting participants, and assisting with study documentation under PI guidance.

Based at Richardson, the position may travel to regional clinics for coverage needs, contributing to monitor visits, data submission, and coordination of trial activities through the continuum of care.