Associate Director, Connect Process

Gilead Sciences

Bay Area, CA, US
Base: bay area $195,670.00 - $253,220.00; other us...
Fully remote
10+ years relevant experience
Bachelor's degree minimum
Fda and ema regulatory knowledge
Gilead Sciences is seeking an Associate Director for the Connect Process, primarily focused on improving clinical operations within a highly regulated environment. The role involves project management, process analysis, and documentation, requiring significant experience in clinical research and strong leadership skills

Job Summary

  • The role supports process analysis and documentation for the Clinical Operations organization within a fast-paced and highly regulated environment.
  • Candidates will oversee process management improvements and ensure alignment with FDA, EMA, and ICH regulations while managing junior staff.
  • Gilead offers competitive compensation ranging from $177,905 to $253,220 depending on location, along with comprehensive benefits including medical, dental, vision, and life insurance.

Matching Summary

Match Score: 85

Gilead Sciences is seeking an Associate Director for the Connect Process, primarily focused on improving clinical operations within a highly regulated environment. The role involves project management, process analysis, and documentation, requiring significant experience in clinical research and strong leadership skills.

Salary

Base: Bay Area $195,670.00 - $253,220.00; Other US Locations $177,905.00 - $230,230.00; Bonus/Equity: Discretionary annual bonus and stock-based incentives eligible

Skills & Requirements

Must-have

  • 10+ years relevant experience
  • Bachelor's degree minimum
  • FDA and EMA regulatory knowledge
  • ICH guidelines and GCP expertise
  • Clinical Operations process management

Nice-to-have

  • Project Management Fundamentals certification
  • Strong change management strategies
  • Microsoft Visio and Project proficiency
  • Experience leading cross-functional teams
  • Ability to navigate ambiguous situations

Key Requirements

  • Bachelor's degree with 10+ years experience OR Masters with 8+ years OR PhD with 5+ years
  • Thorough knowledge of FDA, EMA, ICH guidelines, and Good Clinical Practice (GCP)
  • Fluency with Microsoft Office suite including MS Visio and Project

Work Rights

Not specified

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