Clinical Research Coordinator Ii (regulatory/remote) - Medical Oncology

Washington University in St. Louis

St. Louis, Missouri, US
Base: $52,600.00 - $78,900.00 annually; bonus/equi...
Remote
Managing complex clinical research studies
Ensuring regulatory compliance with federal agencies
Analyzing and reporting adverse events
Washington University in St. Louis is seeking a Clinical Research Coordinator II for medical oncology studies, responsible for managing complex clinical research projects and ensuring compliance with regulatory requirements. The position requires at least two years of clinical research experience and offers a range of benefits, including generous vacation time and tuition support for employees and their families

Job Summary

  • The position assists investigators as a coordinator for complex clinical research studies while ensuring strict adherence to federal and institutional regulations.
  • Responsibilities include managing all phases of the study protocol, analyzing collected clinical data, and making critical decisions regarding participant safety and inclusion.
  • The role offers competitive benefits including up to 22 days of vacation, comprehensive health insurance, and tuition coverage for employees and their families.

Matching Summary

Match Score: 85

Washington University in St. Louis is seeking a Clinical Research Coordinator II for medical oncology studies, responsible for managing complex clinical research projects and ensuring compliance with regulatory requirements. The position requires at least two years of clinical research experience and offers a range of benefits, including generous vacation time and tuition support for employees and their families.

Salary

Base: $52,600.00 - $78,900.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, retirement plan, tuition coverage

Skills & Requirements

Must-have

  • managing complex clinical research studies
  • ensuring regulatory compliance with federal agencies
  • analyzing and reporting adverse events
  • coordinating data collection and coding procedures
  • liaising with sponsoring agencies and participants

Nice-to-have

  • collaborating on manuscript preparation
  • assisting in grant proposal development
  • interpreting scientific literature for planning
  • preparing oral or written progress reports

Key Requirements

  • Bachelor's degree or equivalent combination of education and experience
  • Minimum 2 years of clinical research work experience
  • Basic Life Support certification from American Heart Association or American Red Cross

Work Rights

Not specified

Tailored Resume

Cover Letter