Clinical Operations Asset Lead, Director

GlaxoSmithKline

Base: pln 437,250 to pln 728,750 gross annually; b...
Not specified (assumed flexible based on company culture).
Clinical operations delivery leadership
Portfolio-level strategic clinical research
Cross-functional team management
GlaxoSmithKline (GSK) is seeking a Clinical Operations Asset Lead, Director responsible for the strategic oversight and execution of clinical operations across the asset lifecycle. The ideal candidate will possess extensive experience in leading complex clinical research programs, with strong leadership, stakeholder management, and strategic planning skills

Job Summary

  • The Clinical Operations Asset Lead is accountable for clinical operations delivery across the full asset lifecycle and sets program-level operational strategy to enable scientific execution.
  • The role offers a competitive salary range in Poland with additional benefits including private healthcare, paid leave, life insurance, and pension plans.
  • GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, aiming to positively impact the health of 2.5 billion people by the end of the decade.

Matching Summary

Match Score: 85

GlaxoSmithKline (GSK) is seeking a Clinical Operations Asset Lead, Director responsible for the strategic oversight and execution of clinical operations across the asset lifecycle. The ideal candidate will possess extensive experience in leading complex clinical research programs, with strong leadership, stakeholder management, and strategic planning skills.

Salary

Base: PLN 437,250 to PLN 728,750 gross annually; Bonus/Equity: Eligible for bonus and awards based on performance; Benefits: Private healthcare, additional paid days off, life insurance, private pension plan, fully paid parental and family care leave

Skills & Requirements

Must-have

  • clinical operations delivery leadership
  • portfolio-level strategic clinical research
  • cross-functional team management
  • regulatory pathway navigation
  • asset-level risk and mitigation management
  • vendor selection and oversight

Nice-to-have

  • operational integration of BD deals
  • patient-centric study execution
  • effective cross-functional collaboration
  • innovative clinical development approaches

Key Requirements

  • Bachelor’s degree in science or health-related field
  • extensive portfolio-level clinical research experience
  • expertise in end-to-end clinical development and regulatory landscape
  • proven leadership of complex cross-functional teams
  • experience with multiple regulatory pathways
  • excellent stakeholder management skills

Work Rights

Not specified

Tailored Resume

Cover Letter