Senior Clinical Research Coordinator - Pediatrics Genetics

Washington University

St. Louis, Missouri, US
Base: $62,000.00 - $96,100.00 / annually; bonus/eq...
Rare and genetic diseases
Investigator-initiated studies
Regulatory compliance
This individual oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff

Job Summary

  • This individual oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff.
  • Consents study participants, coordinates study visits alone or in collaboration with clinical research unit staff, IRB submissions including initial, continuing review, and ad hoc submissions for example adverse events (AE), responsible for AE reporting including Medwatch, communications with study monitors and data and safety monitoring boards, and other duties related to conduct of clinical trials.
  • WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.

Matching Summary

This individual oversees and coordinates complex or multi-site clinical research studies; serves as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation, preparation of regulatory compliance and interaction with other departments; may supervise clinical research staff.

Salary

Base: $62,000.00 - $96,100.00 / Annually; Bonus/Equity: Not specified; Benefits: Competitive health insurance, U-Pass, 403(b) Retirement Savings Plan, tuition benefits

Skills & Requirements

Must-have

  • Rare and genetic diseases
  • Investigator-initiated studies
  • Regulatory compliance
  • Participant consent
  • Adverse event reporting

Nice-to-have

  • Motivated individuals
  • Smooth operation
  • New developments

Key Requirements

  • Bachelor's degree or equivalent experience
  • 3 Years Clinical Research Experience
  • Basic Life Support Certification

Work Rights

Not specified

Tailored Resume

Cover Letter