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Senior Associate – Strategic Planning & Operations

3-6 years
Not Disclosed
10 Nov. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Associate – Strategic Planning & Operations

Location: Hyderabad, India
Category: Clinical Development
Job Type: On-Site
Job ID: R-228339

About the Role

Amgen is hiring a Senior Associate – Strategic Planning & Operations to support the Center for Observational Research (CfOR). This position plays a critical role in coordinating operational activities, managing non-interventional research projects, supporting real-world evidence (RWE) studies, and driving process efficiency across global teams.

As demand for real-world evidence continues to grow, this role ensures high-quality execution of operational deliverables, efficient workflows, and seamless collaboration across scientific and cross-functional groups. The position is ideal for professionals with strong project management skills, operational expertise, and an interest in leveraging modern digital and AI tools to improve productivity.

About Amgen and CfOR

Amgen’s Center for Observational Research (CfOR) generates high-quality real-world evidence to support product development, regulatory strategy, and commercialization. CfOR partners with global scientific teams to design and deliver observational research that guides decision-making across a product’s lifecycle.

Key Responsibilities

  • Provide operational support to Observational Research Scientists working on global real-world evidence studies.

  • Manage end-to-end document requirements and support study teams across multiple regions.

  • Facilitate adoption and use of digital platforms such as Smartsheet, Microsoft Teams, Miro, and AI-based tools to enhance productivity and collaboration.

  • Contribute to CfOR’s strategic initiatives, including operational pilots and change-management activities.

  • Maintain high quality standards for all assigned tasks and deliverables.

  • Communicate project status, risks, and issues clearly to internal and cross-functional partners.

  • Support study start-up and close-out processes.

  • Identify process inefficiencies and implement automation or technology-driven improvements.

  • Develop, update, and analyze process flow diagrams to support operational efficiency.

  • Track, reconcile, and update study milestones, timelines, and deliverables within internal systems.

  • Conduct recurring operational meetings with study leads.

  • Coordinate department-wide or cross-functional process improvement initiatives.

  • Manage financial workflows including purchase orders, invoices, payments, and budget tracking using tools such as Anaplan, Ariba, or SAP.

Required Qualifications

  • Bachelor’s degree with 6+ years of experience in Scientific or Operations roles
    OR

  • Master’s degree with 4+ years of experience in Scientific or Operations roles

Preferred Qualifications

  • Minimum 3 years of project management experience, including at least 2 years in pharma/biotech or regulated environments.

  • Experience with budgeting, vendor oversight, and regulated document management systems.

  • Ability to work independently with strong ownership, accountability, and task execution skills.

  • Highly organized with the ability to manage multiple priorities.

  • Strong analytical skills and ability to adopt new tools and workflows quickly.

  • Excellent verbal, written, and presentation communication abilities.

  • Strong interpersonal and collaboration skills with a proactive approach.

  • Proficiency with AI and digital tools including ChatGPT, Copilot, Smartsheet, Miro, SharePoint, MS Teams, and Office 365.

  • Understanding of drug development, commercialization processes, and industry business practices.

  • Knowledge of Good Clinical Practices (GCP), FDA guidelines, and regulatory requirements relevant to clinical and commercial operations.

Why Join Amgen

Amgen offers a collaborative culture committed to scientific excellence, innovation, and operational excellence. You will have the opportunity to support global evidence generation programs while contributing to process improvements that shape the future of CfOR operations.

Apply Now

If you are ready to grow your career within a global scientific environment and support evidence generation that impacts patient care worldwide, apply now to join Amgen’s Center for Observational Research.