Pediatric Oncology Research Coordinator I (Onsite)

Washington University in St. Louis; Missouri; Sur place; USD 49 000 - 74 000; Plein temps

Avantages offerts par ce poste

Vacation up to 22 days

10 recognized holidays

Health insurance

Metro U-Pass

Tuition assistance

Résumé du poste

Washington University in St. Louis is seeking a Clinical Research Coordinator I in Pediatrics Hematology & Oncology to join the Fields lab on the Medical Campus in Saint Louis, MO.

This full-time role supports coordinating complex clinical studies, ensuring protocol compliance, consent processes, participant recruitment, data collection, and timely study completion. The position requires a Bachelor’s degree (or combination with experience) and BLS certification.

Qualifications

• Bachelor’s degree or combination of education and/or experience may substitute for minimum education.
• Basic Life Support certification (Online BLS certifications lacking skills assessment are not sufficient).
• No specific work experience is required for this position.

Responsabilités

• Ensures compliance with protocol guidelines and regulatory requirements.
• Develops informed consent packets and explains study purpose to participants.
• Recruits and enrolls participants based on eligibility criteria.
• Notifies physicians of issues and decisions about protocol adjustments.
• Schedules and facilitates completion of protocol requirements (assessments, lab tests, procedures).
• Collects clinical data, administers/tests, and evaluates results.
• Prepares reports and analyses to communicate progress and conclusions.

Connaissances

Clinical Research

Clinical Study Protocols

Communication

Computer Systems

Interpersonal Communication

Organizing

Research Support

Formation

Bachelor’s degree or combination of education/experience

Description du poste

Washington University in St. Louis is seeking a Clinical Research Coordinator I in Pediatrics Hematology & Oncology to join the Fields lab on the Medical Campus in Saint Louis, MO.

This full-time role supports coordinating complex clinical studies, ensuring protocol compliance, consent processes, participant recruitment, data collection, and timely study completion. The position requires a Bachelor’s degree (or combination with experience) and BLS certification.