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Senior Associate Data Management Two Lab Technicians Smiling

2-3 years
Not Disclosed
10 April 9, 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

 


Position Title:

Senior Associate, Data Management


Location:

India – Hyderabad (On Site)


Job ID:

R-206634


Date Posted:

April 07, 2025


Category:

Regulatory


Job Summary:

The Senior Associate, Data Management will drive key business operations within Veeva RIM Vault, aligning with global regulatory standards like IDMP, EU CTR, and other evolving regulations. This role involves leading regulatory process implementation, supporting system use, and delivering high-quality regulatory information. You will collaborate across functions, offer training, and help shape the future of regulatory operations.


Key Responsibilities:

  • Maintain data in the Regulatory Information Management (RIM) system.

  • Create/archive clinical trial and marketing application submissions and Health Authority correspondence in Amgen’s RIM system.

  • Act as a Data Management SME for cross-functional initiatives.

  • Implement new processes in Veeva Vault, XeVMPD, IDMP, and other key initiatives.

  • Generate and analyze reports for data streamlining.

  • Develop and deliver training content to a global audience.

  • Manage Protocol Amendment New Investigator (PANI) submission updates.

  • Handle 1572 forms for FDA submission.

  • Support with US CPP and EU CMP documentation as needed.

  • Comply with internal SOPs, guidelines, and training documents.


Required Knowledge and Skills:

  • Familiarity with global clinical trial applications, marketing authorizations, and regulatory guidance.

  • Deep understanding of Veeva Vault.

  • Strong communication (written and verbal) in English.

  • Detail-oriented, with critical thinking and independent time management.

  • Ability to work independently with minimal supervision.

  • Team player with strong interpersonal and problem-solving skills.

  • Skilled in relevant software tools.

  • Able to manage business complexity and interdependencies.

  • Experience supporting projects/improvement initiatives.


Preferred Knowledge and Skills:

  • Advanced knowledge of Veeva Vault RIM.

  • Comfortable in dynamic environments and adopting new technologies.

  • Experience in global teams and matrix organizations.

  • Strong task follow-through and team motivation.


Basic Education and Experience (any one of the following):

  • Master’s degree + 1–2 years of related experience

  • Bachelor’s degree + 2–3 years of related experience

  • Associate’s degree + 3–5 years of related experience

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


Preferred Education and Experience:

  • Practical experience with CTIS system