Oncology Prescreening Clinical Research Coordinator

Texas Oncology; Dallas (TX); On-site; USD 55,000 - 75,000; Full time

Job summary

Texas Oncology is seeking a Clinical Research Coordinator to support oncology clinical trials across Texas. The role involves screening patients for eligibility, participating in study visits, and ensuring protocol compliance with SOPs and regulatory standards.

The position offers opportunities for growth across multiple levels (Level 1, 2, or Sr) based on experience, with potential SoCRA/ACRP certification preference.

Qualifications

• Associate's degree in a clinical or scientific field required; Bachelor's preferred.
• Experience in clinical or scientific setting, preferably oncology.
• SoCRA or ACRP certification preferred.

Responsibilities

• Review physician referrals and patient records to identify potential trial candidates.
• Conduct prescreening activities using patient lists, schedules, and data sources.
• Perform trial matching based on eligibility criteria.
• Coordinate with physicians and research staff to refer patients to study teams.
• Maintain documentation of prescreening and referral outcomes in systems.
• Assist with development and maintenance of prescreening workflows and tools.
• Stay updated on trial portfolios and eligibility requirements.
• Participate in training, audits, and process improvements.
• Assist with study documentation and recruitment materials.

Skills

Oncology

Clinical research

Prescreening

Team collaboration

Education

Associate's degree

Bachelor's degree preferred

Tools

SoCRA

ACRP

Job description

Texas Oncology is seeking a Clinical Research Coordinator to support oncology clinical trials across Texas. The role involves screening patients for eligibility, participating in study visits, and ensuring protocol compliance with SOPs and regulatory standards.

The position offers opportunities for growth across multiple levels (Level 1, 2, or Sr) based on experience, with potential SoCRA/ACRP certification preference.