Director, Site Management & Monitoring

Trzdev7

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 complying with AstraZeneca procedural documents and international guidelines

Job Summary

  • The Director, Site Management & Monitoring is responsible for leading a dedicated team to ensure the successful delivery of clinical interventional studies while complying with AstraZeneca procedural documents and international guidelines.
  • This role offers a competitive base salary with bonus and equity opportunities, along with comprehensive benefits including retirement plans, paid leave, and health coverage.
  • The company is committed to building an inclusive environment with equal employment opportunities and provides accommodations for applicants with disabilities or special needs.

Matching Summary

The Director, Site Management & Monitoring is responsible for leading a dedicated team to ensure the successful delivery of clinical interventional studies while complying with AstraZeneca procedural documents and international guidelines.

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 benefits including medical, dental, and vision

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 operations expertise
  • Study documentation and eTMF management

Nice-to-have

  • Cross-functional and global team leadership
  • Coaching and mentorship skills
  • Process improvement and quality focus
  • Collaboration with Medical Affairs
  • Risk-based thinking and problem solving
  • Cultural awareness

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter