Amgen
Clinical Scientist Associate Director – Early Development Inflammation
United States - Remote · Director
Sponsorship not specifiedDetected 1 day ago
Data AnalysisClinical TrialsClinical ResearchResearchLeadershipCommunicationPublic SpeakingGxP
About the role
- Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases.
- With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year.
- Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions.
Responsibilities
- Support set up and execution of early 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.
- 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.
- In this role, the Clinical Scientist Associate Director supports Inflammation early clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities.
- Support appropriate training, recruitment, and development requirements for matrix team resources.
Requirements
- Doctorate degree and 3 years of clinical development experience
- Master's degree and 5 years of clinical development experience
- Bachelor's degree and 7 years of clinical development experience
- Associate's degree and 12 years of clinical development experience
- High school diploma / GED and 14 years of clinical development experience
Nice to have
- 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
- 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
- Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and generation of clinical data outputs
- 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
- Award-winning time-off plans
- careers.amgen.com
Compensation
- 192,597.25USD -260,572.75 USD
Company info
- We are all different, yet we all use our unique contributions to serve patients.
Equal opportunity
- 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.
- Please contact us to request accommodation.
- We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
Visa & Work Authorization
- Sponsorship for this role is not guaranteed.
This listing is sourced directly from Amgen's careers page and normalized into a canonical job model.