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Pv Data Assurance Professional

5 years
Not Disclosed
10 Nov. 12, 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

PV Data Assurance Professional (#1759)

Location: Bengaluru, India
Department: Pharmacovigilance (PV)
Job Type: Full-Time
Apply: [Apply Now]


Purpose and Scope

The PV Data Assurance Professional is responsible for ensuring excellence in Data Assurance across pharmacovigilance (PV) operations, with a focus on the operational aspects of Individual Case Safety Reports (ICSRs) and literature global standards.
The role drives quality, consistency, and operational efficiency across Astellas PV Case Management functions, regions, and case processing vendors.


Key Responsibilities

1. ICSR and Safety Information Processing

  • Implement global ICSR case processing policies and strategies.

  • Create and maintain conventions, tools, and processes for non-medical review and assessment of ICSRs and literature (case intake, data entry, unblinding, quality control, monitoring, etc.).

  • Manage receipt and handling of safety information from co-licensors, partners, affiliates, and third parties.


2. Quality, Data Assurance, Training & Business Information Management

  • Represent the PV Case Management team in inspections, PV audits, and non-PV audits (GMP/GCP) as a Subject Matter Expert (SME) on case quality.

  • Provide justification of Astellas’ case assessments to external bodies during regulatory inspections and authority queries.

  • Review key compliance and quality metrics associated with ICSR assessments and drive continuous quality improvement (in-house and outsourced).


3. Capacity Management, Oversight, and Budget

  • Support capacity management of global case flow through accurate forecasting for developmental and post-marketing activities.

  • Ensure business continuity through effective resource planning and adaptation.

  • Support evaluation, onboarding/training, and performance oversight of outsourced resources.

  • Address and resolve vendor-related issues and escalations.


4. Regional Knowledge, Intelligence & Accountability

  • Maintain up-to-date awareness of regional PV regulations, especially for USA and EU/EEA.

  • Stay informed on global regulatory requirements for intake, review, collation, and reporting of safety information.

  • Ensure PV operations align with local and global authority guidance and institutional standards.


5. People & Organization Management

  • Contribute to building an optimal organizational structure that ensures efficient resource utilization and supports business needs globally.

  • Manage recruitment, performance, and development planning for PV Case Management staff.

  • Foster a culture of collaboration, excellence, and accountability within the PV Case Management function.


6. Strategy Development and Execution

  • Lead and oversee the PV Data Assurance regional team to support global policies and standards ensuring case quality and consistency.

  • Implement and manage PV Case Management operational support tools to improve data accuracy and workflow efficiency.


7. Training

  • Lead training and specialist education initiatives for vendor and PV Case Management teams.

  • Represent PV in cross-functional training sessions to promote pharmacovigilance awareness.

  • Deliver specialist education sessions for internal PV/non-PV staff and external vendor teams.

  • Conduct PV Case Management overview sessions for new Astellas employees involved in Data Assurance.


Required Qualifications

  • Education:

    • Minimum Bachelor’s degree (BA/BS) in a scientific or healthcare discipline.

    • Preferred: Advanced professional degree (e.g., Master’s or higher).

  • Experience:

    • Minimum 5 years of relevant experience in pharmacovigilance (PV) or a combination of PV/Regulatory Affairs (RA)/Quality Assurance (QA), and/or clinical development.

    • Proven leadership experience managing global, multidisciplinary teams.

  • Technical and Regulatory Knowledge:

    • Deep understanding of safety regulations for marketed and investigational products.

    • Excellent knowledge of global health authority requirements (ICH, 21 CFR, FDAAA, EU GVP modules, JP regulations).

    • In-depth understanding of ICSR processing regulatory requirements and guidelines in the assigned region.

    • Proven experience in establishing and maintaining GxP Quality Management Systems.

    • Strong understanding of process management, standards, and training frameworks across the pharmaceutical product lifecycle.


Work Environment

  • Location: Bengaluru, India

  • Department: Pharmacovigilance (PV) – Data Assurance

  • Work Type: Full-time, Onsite/Hybrid