Senior Preclinical Program Lead – Translational Science

Haya Therapeutics SA

Lausanne

Presencial

CHF 150.000 - 190.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

HAYA Therapeutics is seeking an experienced Senior Project Manager to lead IND-enabling nonclinical programs in Lausanne. You will plan translational study designs, coordinate CROs, manage timelines and budgets, and ensure regulatory readiness across global filings.

The role requires in-depth GLP/ICH knowledge, strong cross-functional leadership, and a track record of delivering complex biotech projects on time and within budget.

Formación

  • Bachelor's degree in life sciences or related field; PMP or equivalent preferred.
  • Proven experience in cross-functional project management for biotech/pharma CROs.
  • Strong knowledge of GLP, ICH guidelines and regulatory timelines.

Responsabilidades

  • Lead IND-enabling preclinical study planning (toxicology, PK, in vivo efficacy) and manage study workflows.
  • Coordinate outsourced CRO designs and plans, advising on scientific strategies.
  • Manage vendor relations and act as primary contact with external CROs for timelines, deliverables, and budgets.
  • Anticipate obstacles and align cross-functional teams to remove bottlenecks and accelerate velocity.
  • Develop dashboards and tracking tools for timelines, dependencies, and resources; report to R&D leadership.

Conocimientos

Project management
IND-enabling studies
GLP/ICH compliance
Vendor coordination
Budget management

Educación

Bachelor's degree in life sciences or related field
PMP certification or equivalent

Herramientas

MS Project
Jira
Tableau/Power BI

Descripción del empleo

HAYA Therapeutics is seeking an experienced Senior Project Manager to lead IND-enabling nonclinical programs in Lausanne. You will plan translational study designs, coordinate CROs, manage timelines and budgets, and ensure regulatory readiness across global filings.

The role requires in-depth GLP/ICH knowledge, strong cross-functional leadership, and a track record of delivering complex biotech projects on time and within budget.

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