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Manager Case Processing

Cencora
Cencora
10 years
preferred by company
10 Jan. 6, 2026
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

Manager – Case Processing (Pharmacovigilance)

Location: Noida, India
Employment Type: Full-Time
Experience Required: Minimum 10 years in Pharmacovigilance / Drug Safety Operations
Job ID: R2522051
Category: Consulting / Pharmacovigilance


About Cencora

Cencora is a global leader in healthcare solutions, dedicated to advancing patient safety and creating healthier futures. Our teams deliver world-class pharmacovigilance (PV), regulatory, and clinical operations, ensuring high-quality outcomes and regulatory compliance across international markets.

Joining Cencora means becoming part of a mission-driven organization where innovation, expertise, and collaboration drive meaningful impact on healthcare delivery globally.


Job Overview

The Manager – Case Processing will oversee end-to-end pharmacovigilance operations, ensuring quality, compliance, and operational excellence for assigned PV projects. This role combines strategic leadership, team management, and process optimization to maintain the highest standards in case processing and regulatory reporting.

The ideal candidate has a minimum of 10 years of experience in pharmacovigilance, strong leadership capabilities, and expertise in ICSR processing, regulatory submissions, and quality assurance.


Key Responsibilities

Operational Leadership & Case Management

  • Oversee quality management, compliance, and document management for assigned PV projects

  • Manage ICSR submissions to Health Authorities and client partners

  • Supervise case processing, including data entry, quality control, and case completion

  • Identify potential risks in case processing workflows and develop mitigation strategies

  • Implement robust quality control mechanisms to ensure accuracy and compliance

  • Interface with internal departments such as VDC office, QPPV office, and Compliance to ensure seamless operations

Team Management & Mentorship

  • Act as line manager for assigned PV staff, providing mentorship and guidance

  • Lead training initiatives and ensure training compliance across the PV team

  • Conduct objective setting, performance appraisals, and professional development for staff

  • Support onboarding of new team members and foster a collaborative learning environment

Project Coordination & Process Optimization

  • Manage resource allocation and project coordination for multiple PV assignments

  • Develop and optimize workflow procedures to enhance efficiency, accuracy, and compliance

  • Prepare comprehensive management reports, dashboards, and visual representations of operational performance

  • Draft, review, and maintain QA documents, SOPs, working instructions, templates, and project metafiles

Regulatory & Compliance Oversight

  • Ensure adherence to internal standards, national and international regulations, and client requirements

  • Represent the PV department during for-cause audits, maintenance audits, or regulatory inspections

  • Provide actionable insights and recommendations for continuous process improvement


Qualifications & Experience

  • Education: University degree in Life Sciences or related field

  • Experience: Minimum 10 years in pharmacovigilance operations, with extensive knowledge in ICSR processing, regulatory reporting, and PV project management

  • Strong expertise in case processing workflows, quality assurance, and compliance oversight

  • Excellent written and verbal communication skills, with the ability to provide solutions and recommendations

  • Proven experience in team management, training, and mentorship


Why Join Cencora

  • Lead global pharmacovigilance operations in a dynamic, collaborative environment

  • Drive regulatory compliance, case processing excellence, and patient safety initiatives

  • Access to structured career growth, mentorship, and professional development opportunities

  • Work in an inclusive, equal opportunity workplace committed to employee growth and operational excellence

  • Contribute to meaningful healthcare projects that impact patients and clients worldwide

Cencora is an Equal Opportunity Employer and provides reasonable accommodations for individuals with disabilities in compliance with applicable legal requirements.


Apply now on ThePharmaDaily.com to advance your career as a Manager in Case Processing and Pharmacovigilance with a global healthcare leader.