Senior Clinical Research Coordinator - Pediatrics Genetics

Washington University in St. Louis

St. Louis, Missouri, US
Base: $62,000.00 - $96,100.00 / annually; bonus/eq...
Clinical research studies
Regulatory compliance
Protocol development and management
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 seeks highly motivated individuals who are able to perform duties in a manner consistent with our core mission and guiding principles.

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, retirement plan, tuition benefits

Skills & Requirements

Must-have

  • Clinical research studies
  • Regulatory compliance
  • Protocol development and management
  • Participant consent and monitoring
  • Adverse event reporting

Nice-to-have

  • Collaboration with PIs
  • Manuscript preparation
  • Grant proposal assistance
  • New staff training

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