Clinical Scientist Associate Director, Late Development Oncology

Amgen Inc.

Job Overview

Location

United States - Remote

Job Type

Full-time

Full Job Description

📋 Description

• The Clinical Scientist Associate Director – Late Development Oncology role at Amgen supports late-phase clinical trials in oncology, focusing on protocol development, study execution, data quality, and cross-functional coordination to ensure decision-ready clinical data for regulatory submissions and patient impact.
• Day-to-day responsibilities include supporting trial setup and execution, authoring clinical protocols and regulatory documents, contributing to data management plans and CRF design, reviewing and analyzing clinical trial data, managing collaborators and CROs, anticipating and resolving cross-functional issues, translating clinical strategy into study documents, and supporting team training and development.
• Amgen is a global biotechnology leader pioneering innovative medicines in oncology, inflammation, general medicine, and rare diseases since 1980, with a mission to serve patients with serious illnesses through science-driven, collaborative, and award-winning culture.
• In this role, you will deepen your expertise in late-phase oncology clinical development, lead cross-functional initiatives, contribute to regulatory submissions and scientific publications, and grow as a scientific leader while making a lasting impact on patient lives.

🎯 Requirements

• Doctorate degree and 3 years of clinical development experience, OR Master’s degree and 5 years, OR Bachelor’s degree and 7 years, OR Associate’s degree and 12 years, OR High school diploma/GED and 14 years of clinical development experience
• Preferred: 3 years in pharmaceutical industry with at least 1 year supporting early or late-phase clinical development in oncology or relevant therapeutic area
• Preferred: Experience contributing to clinical trial process improvements within a therapeutic area or study team environment
• Preferred: Strong communication and presentation skills to convey scientific concepts and clinical data to cross-functional teams and leadership, both written and oral
• Preferred: Experience supporting design, monitoring, and implementation of clinical trials in compliance with GCP and regulatory requirements
• Preferred: Working knowledge of study data readout activities including data cleaning, database lock, data extraction, and generation of clinical data outputs

🏖️ Benefits

• Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• Discretionary annual bonus program (or sales-based incentive for field roles)
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible

Skills & Technologies

Junior

Remote

Degree Required

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Amgen Inc.

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About Amgen Inc.

Amgen Inc. is a global biotechnology company headquartered in Thousand Oaks, California. Founded in 1980, it discovers, develops, manufactures, and delivers human therapeutics targeting cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses. Using advanced recombinant DNA and molecular biology techniques, Amgen produces biologic medicines such as Neulasta, Enbrel, and Prolia. The company operates R&D, manufacturing, and distribution facilities worldwide, investing heavily in genomic research to identify novel drug targets. Amgen also partners with academic institutions and smaller biotechs to expand its pipeline, aiming to transform breakthrough science into therapies that significantly improve patients’ lives.

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