Clinical Scientist Associate Director, Late Development Oncology

Amgen

Clinical Scientist Associate Director supporting late-phase oncology clinical development at Amgen. Responsibilities include protocol development, data analysis, and cross-functional collaboration.

Posted 6/19/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $169,793 - $229,721 per yearWebsite

About the role

Key responsibilities & impact

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 and 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 the 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

What you’ll need

Doctorate degree and 3 years of clinical development experience OR Master’s degree and 5 years of clinical development experience OR Bachelor’s degree and 7 years of clinical development experience OR Associate’s degree and 12 years of clinical development experience OR High school diploma / GED and 14 years of clinical development experience
3 years of experience in a pharmaceutical industry setting with at least 1 year supporting early or late-phase clinical development within a relevant therapeutic area or disease indication (oncology preferred)
Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
Strong communication and presentation skills, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral
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.

Benefits

Comp & perks

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible.

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Hard Skills & Tools

clinical developmentclinical trial process improvementsdata management planCRF designdata review oversightregulatory submission documentsclinical data analysisGood Clinical Practicedata cleaningdatabase lock

Soft Skills

strong communication skillspresentation skillsproblem managementcross-functional teamworktraining and development