Amgen Inc. is seeking a Clinical Scientist Associate Director to play a key role in late-phase clinical development. You will focus on study-level implementation and cross-functional coordination to ensure the generation of high-quality, decision-ready clinical data. You will join a collaborative, science-based culture dedicated to serving patients.
What You'll Do
- Support the 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 implement the data management plan, CRF design, and data review oversight.
- Support the review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission.
- Assist the Development Lead and Clinical Scientist Director in medical monitoring and management of collaborators, consultants, and/or Clinical Research Organizations.
- Anticipate and actively manage problems across a broad spectrum of cross-functional teams.
- Work cross-functionally to ensure the clinical strategy is translated into the study concept document, study protocol, and related documents.
- Support appropriate training, recruitment, and development requirements for matrix team resources.
What We're Looking For
- A Doctorate degree and 3 years of clinical development experience
- A Master’s degree and 5 years of clinical development experience
- A Bachelor’s degree and 7 years of clinical development experience
- An Associate’s degree and 12 years of clinical development experience
- A High school diploma / GED and 14 years of clinical development experience
Nice to Have
- 3 years of pharmaceutical clinical drug development experience
- Experience in Autoimmune or inflammation clinical development
- Demonstrated experience contributing to clinical trial process improvements within a therapeutic area or study team environment
- Industry or academic experience supporting late-phase drug development within a relevant therapeutic area or disease indication
- Strong communication and presentation skills to clearly convey scientific concepts and clinical data to cross-functional teams and leadership
- Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice and 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
- 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
Technical Stack
- Spotfire
- Other clinical data analysis tools
Team & Environment
You will work with the study team and clinical leadership, assisting the Development Lead and Clinical Scientist Director.
Benefits & Compensation
- Compensation range: $183,251.00 - $223,386.00 USD
- 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, and flexible spending accounts
- A discretionary annual bonus program
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models where possible
Work Mode
This is a hybrid position. Eligible locations are within the U.S. (excluding Puerto Rico).
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
