Clinical Scientist Associate Director, Late Development Oncology
Amgen
August 20, 2026
Remote friendly (United States)
United States
Clinical Research and Development
Clinical Scientist Associate Director – Late Development
What You Will Do
- Support set up and execution of late phase clinical trials focused on data quality.
- Assist in authoring clinical protocols, Investigators Brochures, and other regulatory documents.
- Provide input into and implement data management plan, CRF design, and data review oversight.
- Support review, analysis, and presentation preparation of clinical trial data for internal decisions, external interactions, and regulatory submission.
- Manage collaborators/consultants/CROs to complete key projects.
- Anticipate and actively manage problems across cross-functional teams.
- Translate clinical strategy into study concept document, study protocol, and related documents.
- Support training, recruitment, and development requirements for matrix team resources.
Basic Qualifications
- Doctorate + 3 years clinical development
OR Master’s + 5 years
OR Bachelor’s + 7 years
OR Associate’s + 12 years
OR High school/GED + 14 years
Preferred Qualifications
- 3 years pharma with 1+ year early or late-phase development in relevant therapeutic area/disease indication (oncology preferred)
- Trial process improvement experience
- Strong written/oral communication and presentation skills
- Experience with GCP and applicable regulatory requirements
- Knowledge of data readout activities (cleaning, database lock, extraction, outputs)
- Regulatory submission document experience and health authority responses
- Contributing author experience (publications/conference presentations)
- Clinical data analysis tools (e.g., Spotfire)
Benefits (Total Rewards Plan, eligibility-based)
- Health/medical/dental/vision, life/disability, flexible spending
- Retirement and Savings Plan (company contributions)
- Discretionary annual bonus (or sales incentive for field reps), stock-based long-term incentives, time off, flexible work models where possible
Application Instructions
- Apply now at careers.amgen.com.
- No application deadline; accepting applications until sufficient or candidate selected.
- You may redact age-identifying information in submitted materials.
What You Will Do
- Support set up and execution of late phase clinical trials focused on data quality.
- Assist in authoring clinical protocols, Investigators Brochures, and other regulatory documents.
- Provide input into and implement data management plan, CRF design, and data review oversight.
- Support review, analysis, and presentation preparation of clinical trial data for internal decisions, external interactions, and regulatory submission.
- Manage collaborators/consultants/CROs to complete key projects.
- Anticipate and actively manage problems across cross-functional teams.
- Translate clinical strategy into study concept document, study protocol, and related documents.
- Support training, recruitment, and development requirements for matrix team resources.
Basic Qualifications
- Doctorate + 3 years clinical development
OR Master’s + 5 years
OR Bachelor’s + 7 years
OR Associate’s + 12 years
OR High school/GED + 14 years
Preferred Qualifications
- 3 years pharma with 1+ year early or late-phase development in relevant therapeutic area/disease indication (oncology preferred)
- Trial process improvement experience
- Strong written/oral communication and presentation skills
- Experience with GCP and applicable regulatory requirements
- Knowledge of data readout activities (cleaning, database lock, extraction, outputs)
- Regulatory submission document experience and health authority responses
- Contributing author experience (publications/conference presentations)
- Clinical data analysis tools (e.g., Spotfire)
Benefits (Total Rewards Plan, eligibility-based)
- Health/medical/dental/vision, life/disability, flexible spending
- Retirement and Savings Plan (company contributions)
- Discretionary annual bonus (or sales incentive for field reps), stock-based long-term incentives, time off, flexible work models where possible
Application Instructions
- Apply now at careers.amgen.com.
- No application deadline; accepting applications until sufficient or candidate selected.
- You may redact age-identifying information in submitted materials.