Clinical Research Coordinator II - Pediatrics Hematology & Oncology

Washington University in St. Louis • St. Louis, MO

93d • $52,600 - $78,900

About The Position

The position involves assisting investigators as a coordinator of complex clinical research studies, potentially managing multiple studies simultaneously. The coordinator acts as a liaison with the school, sponsoring agency, community, and study participants, ensuring compliance with study protocols and regulatory requirements.

Requirements

• Bachelor’s degree or equivalent combination of education and experience.
• 2 years of clinical research experience.
• Basic Life Support certification must be obtained within one month of hire.

Nice To Haves

• One year experience in public health, epidemiological, behavioral medicine, psychological, sociological, anthropological, clinical, or urban planning research.
• Working knowledge of qualitative and/or quantitative data analysis software.
• Communication, organizational, and interpersonal skills.
• Data management and analytic skills, particularly with large data sets.

Responsibilities

• Implement and manage all phases of study/protocol.
• Ensure compliance with protocol guidelines and regulatory agency requirements.
• Establish record-keeping systems.
• Assess and determine participants’ progress in the study.
• Analyze, investigate, and report adverse events.
• Decide when to notify physicians of issues and when to stop participant inclusion.
• Resolve IRB/protocol management issues and recommend corrective actions.
• Serve as a liaison with funding or sponsoring agency.
• Recruit and enroll study participants.
• Determine eligibility based on diagnostic criteria and participant interviews.
• Develop informed consent packets and explain the study purpose to participants.
• Administer tests and evaluate lab and clinical assessments.
• Ensure timely completion of all protocol requirements.
• Evaluate and interpret collected clinical data with the Principal Investigator.
• Prepare presentations or reports on progress trends and provide recommendations.
• Involve in qualitative study projects including interviewing participants and assisting in data analysis.
• Collect clinical data under clinical research protocols.
• Perform other incidental duties as required.

Benefits

• Up to 22 days of vacation, 10 recognized holidays, and sick time.
• Competitive health insurance packages.
• Free Metro transit U-Pass for eligible employees.
• Defined contribution (403(b)) Retirement Savings Plan with university contributions.
• Wellness challenges, annual health screenings, mental health resources, and employee assistance program.
• 4 weeks of caregiver leave.
• Tuition coverage for employees and their families.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Bachelor's degree