Roles & Responsibilities
Participate in technical discussions related to the Risk base Quality Management (RBQM) system(s) within Clinical Trial Operations and Site Engagement (CTOSE) product team.
Take ownership of complex software projects from conception to deployment. Build technical solution as per implementation project plan by working with various members of the product team and business partners.
Possesses strong knowledge and hands-on expertise on application/system integrations and backend development
Possesses strong rapid prototyping skills and can quickly translate concepts into working code along with managing software delivery scope, risk, and timeline.
Contribute to both front-end & back-end development and Integrations using cloud technology & generative AI.
Conduct user acceptance testing with the customer, including coordination of all feedback, resolution of issues, and acceptance of the study
Support requirements gathering and specification creation process for the development work.
Communicate potential risks and contingency plans with project management to ensure process compliance with all regulatory and Amgen procedural requirements
Participate and contribute to process product or standard methodologies initiatives and support developers and testers during the project lifecycle.
Define, author, and present various architecture footprints i.e. Business, Logical, Integration, Security, Infrastructure, etc.
Create and maintain detailed documentation on software architecture, design, deployment, disaster recovery, and operations.
Conduct code reviews to ensure code quality and adherence to best practices.
Identify and resolve technical challenges/bugs/issues effectively within deadlines.
Work closely with multi-functional teams, including product management, design, and QA, to deliver high-quality software on time.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients.
Basic Qualifications
Master's or Bachelor’s degree with 8 - 12 years of experience in Computer Science
Preferred Qualifications
Solid technical background, including understanding software development processes, application/system integrations, databases, and cloud-based content systems.
Strong problem solving, analytical skills; Ability to learn quickly; Excellent communication (verbal & written) and interpersonal skills.
Good knowledge of scripting language (Python), SQL queries, markup languages (XML, JSON), integration tools (mulesoft, databricks, APIs) and familiarity with API-driven content delivery.
Agile/Scrum experience with demonstrated success managing product backlogs and delivering iterative product improvements.
Strong knowledge of Pharma domain & Clinical Trial processes
Experience with product backlog management (e.g., Jira) and collaboration tools.
Good-to-Have Skills
Experience with structured content management, content models, and modular content creation.
Knowledge of Risk based Quality Management for Clinical Trials
Understanding of international pharmaceutical regulatory submission guidelines and processes (eCTD, ICH, CDS, USPI etc.).
Strong understanding of cloud platforms (e.g., AWS, GCP, Azure) and containerization technologies (e.g., Docker, Kubernetes).
Experience with data processing tools like Hadoop, Spark, or similar.
Basic understanding of GenAI solutions.
Good communication skills, with the ability to convey complex technical concepts.
Soft Skills
Excellent analytical and troubleshooting skills.
Strong verbal and written communication skills
Ability to work effectively with global, virtual teams.
High degree of initiative and self-motivation.
Ability to manage multiple priorities successfully.
Team-oriented, with a focus on achieving team goals.
Strong presentation and public speaking skills.
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
Apply now for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
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.
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. Please contact us to request accommodation.
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Please note that you should be in your current position for at least 18 months before applying to internal positions. Staff must notify their current manager if invited for an interview. In addition, Staff are ineligible to apply for open positions if (a) their performance is currently being managed on a performance improvement plan (PIP) or other locally utilized formal coaching document or (b) their most recent performance rating was not a “Partially Meets Expectations” or higher. Please visit our Internal Transfer Guidelines for more detailed information
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