Director, Site Management & Monitoring

Trzdev15

Base: $171,622.40 - $257,433.60 usd annual; bonus/...
Clinical interventional studies delivery
Ich-gcp compliance
Line management and resource planning
The Director, Site Management & Monitoring is responsible for ensuring the successful delivery of all clinical interventional studies in accordance with agreed resources, budgets, and timelines, complying with international guidelines and local regulations

Job Summary

  • The Director, Site Management & Monitoring is responsible for ensuring the successful delivery of all clinical interventional studies in accordance with agreed resources, budgets, and timelines, complying with international guidelines and local regulations.
  • 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 include 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 delivery of all clinical interventional studies in accordance with agreed resources, budgets, and timelines, complying with international guidelines and local regulations.

Salary

Base: $171,622.40 - $257,433.60 USD Annual; Bonus/Equity: Short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: Qualified retirement program, paid vacation and holidays, paid leaves, health benefits

Skills & Requirements

Must-have

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

Nice-to-have

  • High-performing team culture
  • Continuous improvement of processes
  • Cross-functional collaboration
  • Risk-based thinking
  • Cultural awareness

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter