Global Clinical Program Lead

HAYA Therapeutics

Lausanne

Vor Ort

CHF 140.000 - 190.000

Vollzeit

14 Tage+

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Zusammenfassung

HAYA Therapeutics in Lausanne leads a dynamic clinical program management role focused on guiding early-stage assets from nomination through clinical phases. You will coordinate clinical development activities across clinical, regulatory, safety, and quality teams to ensure timely, budget-compliant delivery of assets.

The ideal candidate brings strong regulatory and operational planning experience, hands-on budget management, and excellent cross-functional leadership to drive strategic

Qualifikationen

  • Experience guiding early-stage therapeutic assets through IND transitions into active clinical development.
  • Strong knowledge of global drug development plans and regulatory pathways.
  • Proven ability to manage budgets, forecasts, and vendor relationships for clinical trials.
  • Analytical problem-solving and robust program documentation (ADR logs).
  • Excellent communication and negotiation skills for cross-functional alignment and leadership.

Aufgaben

  • Lead cross-functional program activities across clinical, nonclinical, biomarkers, CMC, regulatory and quality to ensure milestones are met.
  • Consolidate program timelines and operational plans to resolve bottlenecks and keep execution on target.
  • Coordinate supply schedules and data deliverables to ensure availability of trial materials and safety data.
  • Incorporate guidance from regulatory and QA to maintain compliance throughout the lifecycle.
  • Manage program scope, budgets, and monthly forecasts with variance tracking.
  • Maintain ADR log and ensure visibility for senior leadership.

Kenntnisse

Clinical program mgmt
Regulatory knowledge
Cross-functional leadership
Budget management
Risk management
MS Project
Excel
PowerPoint
Outlook

Tools

MS Project
Excel
PowerPoint
Outlook

Jobbeschreibung

HAYA Therapeutics in Lausanne leads a dynamic clinical program management role focused on guiding early-stage assets from nomination through clinical phases. You will coordinate clinical development activities across clinical, regulatory, safety, and quality teams to ensure timely, budget-compliant delivery of assets.

The ideal candidate brings strong regulatory and operational planning experience, hands-on budget management, and excellent cross-functional leadership to drive strategic

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