Oncology Clinical Research Coordinator - Prescreening

US Oncology Network-wide Career Opportunities; Dallas (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401k with company match

Tuition reimbursement

Wellness program

Employee assistance program

Paid time off

Job summary

Texas Oncology is seeking aClinical Research Coordinator to support the Dallas Region in the Oncology Clinical Research department. Responsibilities include screening patients for eligibility, obtaining informed consent, and coordinating study visits in accordance with protocol.

The role offers opportunities across Level 1, 2, or Sr depending on experience, with a comprehensive benefits package and a focus on compliance with GCP, SOPs, and regulatory requirements.

Qualifications

• Associate's degree in a clinical or scientific discipline required; Bachelor's degree preferred.
• Minimum one year of experience in a clinical or scientific discipline, preferably oncology.
• Level 2 requires minimum five years of experience in a clinical or scientific discipline, preferably oncology; SoCRA or ACRP certification preferred.
• Level Sr requires minimum seven years of experience in a clinical or scientific discipline; five years oncology/research experience preferred.

Responsibilities

• Screen potential patients for protocol eligibility and enroll patients in trials.
• Assist with patient care in protocol compliance and manage data collection and reporting.
• Review patient condition changes, adverse events, and concomitant medications with physicians.
• Participate in training, monitoring, and auditing activities and interact with monitors.

Skills

Clinical research

Oncology experience

Regulatory knowledge

SoCRA/ACRP certification

Education

Associate degree in clinical or scientific discipline

Bachelor's degree preferred

Job description

Texas Oncology is seeking aClinical Research Coordinator to support the Dallas Region in the Oncology Clinical Research department. Responsibilities include screening patients for eligibility, obtaining informed consent, and coordinating study visits in accordance with protocol.

The role offers opportunities across Level 1, 2, or Sr depending on experience, with a comprehensive benefits package and a focus on compliance with GCP, SOPs, and regulatory requirements.