Manager, CSAR – Custom function Programming
Amgen · Hyderabad, India
IT & SoftwareFull-timeCompany career page
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Role summary
Amgen seeks a Manager for Custom function Programming and Study Design to lead clinical trial database development and electronic data capture implementation. The role requires expertise in clinical systems, regulatory compliance, and cross-functional collaboration to support drug development initiatives.
What they're looking for
- Bachelor's degree in life science, computer science, business administration, or related field plus 9–12 years experience
- Expertise in clinical trial database systems, edit check development, and custom function programming
- Proficiency in electronic data capture platforms such as Rave EDC or Veeva EDC
- Strong knowledge of Good Clinical Practice, data management processes, and regulatory requirements
- Demonstrated experience leading cross-functional teams and managing vendor relationships
- Advanced degree preferred in life science, computer science, statistics, or related discipline
What you'll be doing
- Build, program, and maintain clinical trial databases adhering to Amgen standards and regulatory procedures
- Provide technical support and programming guidance to clinical study teams and cross-functional staff
- Identify and implement system enhancements, tools, and emerging technologies to optimize development cycles
- Develop, review, and maintain policies, standard operating procedures, and technical documentation
- Support audit preparation and response activities for internal and external regulatory inspections
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.