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Clinical Scientist Director – Late Development Oncology

amgen

Novo
Senior 105,822 - 169,745 EUR/ano 🇬🇧 English
Spotfire

Descrição do cargo

About the role

Amgen is hiring a Clinical Scientist Director for late development oncology. The role supports late-phase clinical development by turning scientific and clinical strategy into actionable execution across clinical trials, with hands-on oversight of protocol execution, medical data review and clinical data quality so that decision-ready data is delivered.

Key responsibilities

  • Serve as clinical and scientific subject-matter expert for the assigned therapeutic area and disease indication, focusing on protocol execution and data integrity
  • Contribute to medical monitoring and assess subject-level clinical data to identify trends, risks and emerging issues
  • Present information internally and externally, and manage problems across cross-functional teams
  • Guide the selection and management of collaborators, consultants and CROs for key projects
  • Help turn clinical strategy into the study concept document, study protocol and related documents, and ensure protocol integrity and governance approval
  • Provide clinical input into trial design, delivery, data review and interpretation of results
  • Review and analyse trial data for accuracy, completeness and compliance with protocol and regulatory requirements
  • Carry out data quality assessments under a data monitoring plan

Required profile

  • Basic: doctorate with 4 years of life sciences/healthcare experience, or master's with 7 years, or bachelor's with 9 years
  • Preferred: 5 years of pharmaceutical clinical drug development experience
  • Preferred: proven track record of clinical trial process improvement
  • Preferred: industry or academic experience in late-phase oncology drug development
  • Preferred: experience designing, monitoring and running oncology trials and interpreting results under GCP
  • Preferred: experience in study data readout (cleaning, database lock, extracts, outputs)
  • Preferred: drafting clinical regulatory submissions and responses, and contributing to scientific publications and conference presentations
  • Preferred: clinical data analysis with Spotfire or similar tools

Required skills

  • Good written and oral communication and presentation skills
  • Experience with clinical trial data analysis tools such as Spotfire

What we offer

  • Annual salary range depending on country: Portugal 105,822 to 143,171 EUR, Spain 138,883 to 169,745 EUR, Poland 553,912 to 677,004 PLN
  • Health, dental and vision coverage, life and disability insurance, and a retirement savings plan with company contributions
  • Discretionary annual bonus or sales-based incentive plan, stock-based long-term incentives
  • Award-winning time-off plans and flexible work models, including remote and hybrid options where possible

Questions fréquentes

Le salaire proposé pour ce poste est de 106-170k EUR par an. Le détail figure dans l'annonce.
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