Director, Site Management & Monitoring

Tryzenoya

Base: $171,622.40 - $257,433.60 usd annually; bonu...
Clinical study site management
Team leadership and performance management
Compliance with ich-gcp and local regulations
The Director, Site Management & Monitoring is responsible for leading a dedicated team to ensure the successful delivery of clinical interventional studies while maintaining compliance with international guidelines and local regulations

Job Summary

  • The Director, Site Management & Monitoring is responsible for leading a dedicated team to ensure the successful delivery of clinical interventional studies while maintaining compliance with international guidelines and local regulations.
  • The role offers a competitive salary range with bonus and equity opportunities, comprehensive benefits including retirement plans, paid leave, and health coverage, and supports an inclusive work environment.
  • This position requires collaboration with multiple stakeholders including Medical Affairs, Country Heads, and study teams to drive quality outcomes and continuous improvement in clinical study operations.

Matching Summary

The Director, Site Management & Monitoring is responsible for leading a dedicated team to ensure the successful delivery of clinical interventional studies while maintaining compliance with international guidelines and local regulations.

Salary

Base: $171,622.40 - $257,433.60 USD annually; Bonus/Equity: Short-term incentive bonus and equity-based long-term incentive program eligibility; Benefits: Retirement program, paid vacation and holidays, health coverage

Skills & Requirements

Must-have

  • Clinical study site management
  • Team leadership and performance management
  • Compliance with ICH-GCP and local regulations
  • Resource and budget oversight
  • Clinical trial monitoring and documentation
  • Cross-functional collaboration
  • Process improvement in clinical operations

Nice-to-have

  • Coaching and mentorship skills
  • Cultural awareness in global teams
  • Effective communication and teamwork
  • Risk-based thinking and problem solving
  • Ability to travel nationally and internationally
  • Driving license if required

Key Requirements

  • Bachelor’s degree in life sciences or related discipline
  • 5+ years pharmaceutical industry experience
  • Knowledge of drug development and GxP processes
  • Familiarity with ICH-GCP and local regulations
  • Business-level fluency in English
  • Valid driving license if required by country
  • Ability to travel nationally/internationally

Work Rights

Not specified

Tailored Resume

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