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Senior Associate Data Management

2-3 years
Not Disclosed
10 May 1, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Job Title: Senior Associate, Data Management

Location: India – Hyderabad (On Site)
Job ID: R-206634
Date Posted: April 7, 2025
Category: Regulatory
Company: Amgen


Job Summary

Amgen is seeking a Senior Associate in Data Management to join the team in Hyderabad. In this role, you will leverage your expertise in Veeva RIM Vault to drive business operations, ensuring regulatory compliance with emerging global standards like IDMP and EU CTR. You will support the implementation of new processes, ensure efficient and high-quality regulatory data management, and contribute to training and the development of data standards. Your role will be critical in maintaining regulatory compliance across global markets while streamlining data management processes.


Key Responsibilities

  • Maintain and manage data within Regulatory Information Management (RIM) systems like Veeva Vault

  • Create and archive clinical trial and marketing application submissions and Health Authority correspondence

  • Lead and collaborate on cross-functional initiatives to implement regulatory processes, ensuring compliance with global standards

  • Support the implementation of regulatory initiatives like XeVMPD, IDMP, and others

  • Develop and deliver training materials and presentations for global teams

  • Manage protocol amendment submissions and 1572 forms for FDA submission

  • Support global data management efforts related to US CPP and EU CMP during peak workload periods

  • Adhere to Amgen’s processes, policies, and guidelines


Required Skills and Experience

  • In-depth understanding of Veeva Vault system

  • Strong familiarity with Global Clinical Trial Applications, Marketing Authorizations, and Regulatory Guidance

  • Good written and verbal communication skills in English

  • Critical thinking and problem-solving skills

  • Independent time management and prioritization skills

  • Ability to work in demanding situations with tact, diplomacy, and respect

  • Experience in supporting projects and improvement initiatives


Preferred Knowledge and Skills

  • Advanced knowledge of Veeva Vault RIM

  • Experience working in global teams and matrix organizations

  • Familiarity with CTIS system and global regulatory landscape


Education and Experience

  • Master’s degree with 1-2 years of directly related experience

  • Bachelor’s degree with 2-3 years of related experience

  • Associate’s degree with 3-5 years of directly related experience

  • High school diploma/GED with 5+ years of related experience


Why Join Amgen?

  • Global impact: Drive regulatory compliance in the fast-evolving biotech landscape

  • Collaborative culture: Be part of a dynamic team with a shared commitment to improving patient outcomes

  • Career development: Work in an environment that fosters continuous learning and growth


How to Apply

Visit: careers.amgen.com