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Clinical Scientist Associate Director - Late Development, Oncology

Portugal, Lisbon · Job Posted March 20, 2026
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Job Description

In this role, the Clinical Scientist Associate Director supports late-phase clinical development by contributing to protocol development, study start up, data review and monitoring and analysis activities. Working collaboratively with the study team and clinical leadership, this role focuses on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data.

Job Responsibility

  • Support set up and execution of late phase clinical trials with a focus on data quality
  • Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
  • Provide input into & implementation of data management plan, CRF design, and data review oversight
  • Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
  • Assists Development Lead and Medical Sciences Director in medical monitoring and management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
  • Anticipate and actively manage problems across a broad spectrum of cross-functional teams
  • Work cross functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
  • Support appropriate training, recruitment, and development requirements for matrix team resources

Requirements

  • Doctorate degree and 3 years of life sciences/healthcare experience
  • Master’s degree and 5 years of life sciences/healthcare experience
  • Bachelor’s degree and 7 years of life sciences/healthcare experience
  • 3 years of pharmaceutical clinical drug development experience
  • Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
  • Industry or academic experience supporting early or late-phase drug development within a relevant therapeutic area or disease indication
  • Strong communication and presentation skills in English
  • Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements
  • Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and generation of clinical data outputs
  • Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance
  • Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences
  • Experience in clinical data analysis such as Spotfire or other data analysis tools

What we offer

  • Vast opportunities to learn, develop, and move up and across our global organization
  • Diverse and inclusive community of belonging, where colleagues are empowered to bring ideas to the table, take risks, and act
  • Generous AMGEN Total Rewards Plan comprising healthcare, finance, wealth, and career benefits
  • Flexible work arrangements

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