Associate Director, Clinical Affairs

BD

Irvine, CA, USA
Base: $175,800.00 - $281,300.00 usd annual; bonus/...
Fully remote
End-to-end clinical study oversight
Regulatory compliance and safety reporting
Managing cross-functional teams
This senior leadership role provides end-to-end oversight of complex clinical studies and registries within a highly regulated medical technology environment

Job Summary

  • This senior leadership role provides end-to-end oversight of complex clinical studies and registries within a highly regulated medical technology environment.
  • The position requires managing managers and professionals across multiple large-scale initiatives while ensuring regulatory compliance, data integrity, and successful study execution.
  • Candidates must have at least 10 years of professional clinical research experience and 5 years of people management experience in a regulated setting.

Matching Summary

This senior leadership role provides end-to-end oversight of complex clinical studies and registries within a highly regulated medical technology environment.

Salary

Base: $175,800.00 - $281,300.00 USD Annual; Bonus/Equity: Not specified; Benefits: Comprehensive Total Rewards program including performance-based culture

Skills & Requirements

Must-have

  • End-to-end clinical study oversight
  • Regulatory compliance and safety reporting
  • Managing cross-functional teams
  • Risk assessment and mitigation strategies
  • Device accountability processes

Nice-to-have

  • IRB interaction escalation experience
  • Live case support with physicians
  • Talent development plan creation
  • Negotiation with external parties
  • High-impact program delivery

Key Requirements

  • Bachelor's Degree in life sciences
  • 10+ years clinical research or operations experience
  • 5+ years people management experience
  • Experience leading concurrent complex projects
  • Understanding of device-related event oversight

Work Rights

Not specified

Tailored Resume

Cover Letter