Oncology Clinical Research Coordinator, Prescreening

US Oncology Inc.; Dallas, Northern (TX, KY); On-site; USD 55,000 - 85,000; Full time

Job summary

Texas Oncology seeks a Clinical Research Coordinator to support the Dallas Region in oncology clinical research. Typical hours are Mon-Fri 8:30am-5:00pm. The role involves screening patients, enrolling in trials, and coordinating study activities with physicians and sponsors.

Level 1/2/Sr levels depend on experience. Ideal candidates have an Associate's degree (Bachelor's preferred) and 1+ year in a clinical/scientific setting, with SoCRA/ACRP certification preferred.

Qualifications

• Associate's degree required; Bachelor's preferred.
• Minimum one year of experience in a clinical or scientific discipline, preferably oncology.
• Five years of experience in a clinical or scientific discipline required for Level 2, oncology preferred.
• SoCRA or ACRP certification preferred.

Responsibilities

• Screen potential patients for protocol eligibility, present trial concepts, enroll patients in trials.
• Assist with patient care per protocol, maintain investigational drug accountability, participate in data collection and reporting.
• Review patient changes with physicians, document findings, monitor for adverse events.
• Participate in training programs, monitoring and auditing, may interact with sponsors onsite.
• Assist in collection and maintenance of regulatory documents per SOPs and regulations.
• May assist in packing/shipping of lab specimens; Hazmat and/or IATA training may be required.

Education

Associate's degree in clinical or scientific discipline

Bachelor's degree preferred

SoCRA or ACRP certification

Job description

Texas Oncology seeks a Clinical Research Coordinator to support the Dallas Region in oncology clinical research. Typical hours are Mon-Fri 8:30am-5:00pm. The role involves screening patients, enrolling in trials, and coordinating study activities with physicians and sponsors.

Level 1/2/Sr levels depend on experience. Ideal candidates have an Associate's degree (Bachelor's preferred) and 1+ year in a clinical/scientific setting, with SoCRA/ACRP certification preferred.