Oncology Clinical Research Coordinator – Prescreening

The US Oncology Network; Dallas (TX); On-site; USD 52,000 - 68,000; Full time

Job summary

Texas Oncology seeks a Clinical Research Coordinator to support the Dallas Region in the Oncology Clinical Research department. Typical hours are Mon-Fri, 8:30am-5:00pm; position can be Level 1, 2 or Sr depending on experience.

The role involves screening patients, coordinating visits, ensuring protocol compliance, and collaboration with physicians under US Oncology SOPs and regulatory standards. On-site work in a fast-paced oncology setting.

Qualifications

• Associate's degree required, Bachelor's preferred.
• Minimum one year of experience in a clinical or scientific field, oncology preferred.
• Minimum five years of experience in a clinical or scientific field, oncology preferred; SoCRA/ACRP certification preferred.
• Minimum seven years of experience in a clinical or scientific field; oncology/research preferred; SoCRA/ACRP strongly preferred.

Responsibilities

• Screen potential patients for protocol eligibility and present trial concepts to patients.
• Obtain informed consent, enroll patients in trials, and assist with patient care per protocol.
• Document patient conditions, adverse events, concomitant medications, and responses to study drugs.
• Assist with training, monitoring, and audits; interact with sponsors/monitors on-site as needed.
• Maintain regulatory documents per SOPs and applicable regulations.
• May assist in packing/shipping of lab specimens; may require Hazmat/IATA training.

Skills

Clinical research coordination

Oncology experience

Documentation & data entry

Education

Associate's degree in clinical/scientific discipline

Bachelor's degree preferred

Tools

SoCRA certification

ACRP certification

Job description

Texas Oncology seeks a Clinical Research Coordinator to support the Dallas Region in the Oncology Clinical Research department. Typical hours are Mon-Fri, 8:30am-5:00pm; position can be Level 1, 2 or Sr depending on experience.

The role involves screening patients, coordinating visits, ensuring protocol compliance, and collaboration with physicians under US Oncology SOPs and regulatory standards. On-site work in a fast-paced oncology setting.