Associate Director, Clinical Operations

Added
9 minutes ago
Type
Full time
Salary
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Related skills

forecasting vendor management regulatory submissions ich-gcp cro management

📋 Description

  • Lead overall management of multiple clinical trials from Phase II–III.
  • Ensure adherence to ICH-GCP, SOPs, and regulatory guidelines.
  • Oversee CROs and vendors to meet milestones and quality.
  • Communicate project status to stakeholders and escalate issues.
  • Plan budgets, timelines, and risk mitigation across programs.

🎯 Requirements

  • BA/BS in life sciences or equivalent.
  • 8+ years clinical research experience.
  • 3+ years leading global projects.
  • 2+ years Biotech industry preferred.
  • Knowledge of pharma processes and regulatory frameworks.
  • Strong cross-functional leadership and communication.
  • Experience budgeting and managing program-level budgets.

🎁 Benefits

  • Salary range: $180,000 - $195,000 per year.
  • Base pay, bonus, equity grant opportunities.
  • Health, welfare, and retirement benefits.
  • Three weeks PTO, two shutdown weeks, paid sick leave.
  • Professional development resources and growth.
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