Director, Site Management & Monitoring

Trzdev37

$171,622.40 - $257,433.60 usd annual; bonus/equity...
Clinical interventional studies delivery
Ich-gcp compliance
Line management and resource planning
The Director, Site Management & Monitoring is responsible for ensuring the successful performance and management of the assigned team, guaranteeing the successful delivery of all clinical interventional studies

Job Summary

  • The Director, Site Management & Monitoring is responsible for ensuring the successful performance and management of the assigned team, guaranteeing the successful delivery of all clinical interventional studies.
  • This role oversees a dedicated group or groups of staff, taking accountability for line management, resource planning and utilization, budget oversight, objective setting, and performance monitoring.
  • Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage.

Matching Summary

The Director, Site Management & Monitoring is responsible for ensuring the successful performance and management of the assigned team, guaranteeing the successful delivery of all clinical interventional studies.

Salary

$171,622.40 - $257,433.60 USD Annual; Bonus/Equity/Retirement/Commission opportunity; Comprehensive benefits package

Skills & Requirements

Must-have

  • Clinical interventional studies delivery
  • ICH-GCP compliance
  • Line management and resource planning
  • Budget oversight and performance monitoring
  • Study site identification and initiation
  • Electronic Trial Master File (eTMF) maintenance

Nice-to-have

  • Fostering cohesive team spirit
  • Contributing to regional initiatives
  • Driving quality outcomes
  • Cross-functional, virtual, and global leadership
  • Risk-based thinking and problem solving

Key Requirements

  • Bachelor’s degree in related discipline or equivalent
  • 5+ years experience in pharmaceutical industry
  • Knowledge of drug development process and GxP
  • Familiarity with ICH-GCP and country regulations
  • Clinical Study Management experience

Work Rights

Not specified

Tailored Resume

Cover Letter