Associate Director, Clinical Operations

Nuvalent

Remote, United States
Base: $171,000 – $200,000 usd; bonus/equity: not s...
Remote
8 years of clinical operations experience
Phase 2 oncology clinical trial management
Ich-gcp guidelines knowledge
Nuvalent is seeking an Associate Director of Clinical Operations to lead Phase 2 clinical studies, ensuring compliance with regulatory guidelines while managing cross-functional teams and vendor relationships. The ideal candidate will have extensive experience in clinical operations within the biotech or pharmaceutical industry, strong project management skills, and a collaborative mindset

Job Summary

  • The role involves leading a Phase 2 registrational clinical study with responsibilities including inspection readiness, contract negotiation, and budget management.
  • Nuvalent is an early-stage biotech company focused on creating selective medicines for cancer patients with deep expertise in chemistry and drug discovery.
  • The position offers a comprehensive benefit package including medical, dental, vision insurance, 401(k) retirement savings plan, and generous paid time off.

Matching Summary

Match Score: 85

Nuvalent is seeking an Associate Director of Clinical Operations to lead Phase 2 clinical studies, ensuring compliance with regulatory guidelines while managing cross-functional teams and vendor relationships. The ideal candidate will have extensive experience in clinical operations within the biotech or pharmaceutical industry, strong project management skills, and a collaborative mindset.

Salary

Base: $171,000 – $200,000 USD; Bonus/Equity: Not specified; Benefits: Medical, dental, vision, 401(k), PTO

Skills & Requirements

Must-have

  • 8 years of Clinical Operations experience
  • Phase 2 oncology clinical trial management
  • ICH-GCP guidelines knowledge
  • CRO and vendor oversight skills
  • Study budget forecasting and management

Nice-to-have

  • Leadership in regulatory inspections
  • Experience with global trials
  • Ability to work in remote environment
  • Cross-functional team collaboration
  • Risk assessment and contingency planning

Key Requirements

  • Bachelor's degree or higher in scientific discipline
  • Minimum 8 years Clinical Operations experience
  • Extensive knowledge of ICH-GCP guidelines
  • Leadership experience in regulatory inspections preferred

Work Rights

Not specified

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