Instagram
youtube
Facebook

Senior Associate Data Management

5+ years
Not Disclosed
10 April 22, 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

 


Senior Associate Data Management

Location: Hyderabad, India
Work Location Type: On Site
Job ID: R-206635
Date Posted: April 22, 2025
Category: Regulatory


About the Role:

The Senior Associate, Data Management, plays a crucial role in driving key business operation initiatives within Veeva RIM Vault, ensuring compliance with global regulatory requirements such as IDMP, EU CTR, and other emerging regulations. This role involves leading regulatory process implementation, promoting system adoption, supporting regulatory data management, and delivering high-quality regulatory information to global teams.


Roles & Responsibilities:

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

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

  • Serve as a subject matter expert (SME) in Data Management for cross-functional collaborative initiatives.

  • Implement new processes within Veeva Vault, XeVMPD, IDMP, and other regulatory initiatives to align with global regulatory standards.

  • Create, run, and analyze reports for data streamlining projects.

  • Develop and deliver training materials and presentations to global audiences.

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

  • Manage 1572 forms for FDA submissions.

  • Support US Certificate of Pharmaceutical Product (CPP) and EU Certificate of Medicinal Product (CMP) processes during peak workload periods.

  • Adhere strictly to Amgen processes, policies, guidelines, SOPs, and training documentation.


Required Knowledge and Skills:

  • Familiarity with Global Clinical Trial Applications, Marketing Authorizations, Regulations, and Regulatory Guidance.

  • In-depth understanding of the Veeva Vault system.

  • Strong written and verbal communication skills.

  • Detail-oriented with independent time management and prioritization skills.

  • Ability to work efficiently with minimal supervision.

  • Strong critical thinking, analytical, and problem-solving skills.

  • Proficiency in appropriate software and reporting tools.

  • Ability to work collaboratively under demanding situations with a positive, respectful attitude.

  • Strong understanding of business complexity and project inter-dependencies.

  • Ability to influence consensus in cross-functional, global teams.

  • Fluent in English (oral and written communication).

  • Experience supporting projects and improvement initiatives.


Preferred Knowledge and Skills:

  • Advanced knowledge of Veeva Vault RIM.

  • Adaptability to dynamic environments and openness to adopting new technologies.

  • Experience working in global teams and matrix organizations.

  • Ability to follow through on tasks and motivate others to meet deadlines.

  • Practical experience with CTIS (Clinical Trials Information System) is preferred.


Education and Experience:

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

  • Bachelor’s degree with 2–3 years of directly related experience
    OR

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

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