Associate Director, Clinical Program Management

Takeda UK

Bengaluru, India
10+ years pharmaceutical industry experience
7+ years clinical study management oversight
Phase 1, 2, 3 global study execution
Lead the operational strategy and execution of clinical studies while ensuring compliance with ICH GCP and quality standards

Job Summary

  • Lead the operational strategy and execution of clinical studies while ensuring compliance with ICH GCP and quality standards.
  • Collaborate with key investigators and cross-functional teams to translate Clinical Development Plans into feasible operational strategies.
  • Oversee strategic CRO partners and manage clinical budgets to ensure studies are delivered on schedule and within financial constraints.

Matching Summary

Lead the operational strategy and execution of clinical studies while ensuring compliance with ICH GCP and quality standards.

Skills & Requirements

Must-have

  • 10+ years pharmaceutical industry experience
  • 7+ years clinical study management oversight
  • Phase 1, 2, 3 global study execution
  • ICH GCP and local regulatory compliance
  • Strategic CRO partner management
  • Clinical budget planning and validation

Nice-to-have

  • Cross-regional collaboration expertise
  • Innovative operational efficiency strategies
  • Talent development and mentoring skills
  • Therapeutic area diversity experience
  • Conflict resolution in negotiations

Key Requirements

  • Bachelor's degree required; Life Sciences preferred
  • Fluency in English and local native language
  • Experience in multiple therapeutic areas
  • Global/international study program experience

Work Rights

Not specified

Tailored Resume

Cover Letter