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Specialist, Pharmacovigilance Epidemiology & Risk Management

Cencora
Cencora
0-2 years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Specialist – Pharmacovigilance Epidemiology & Risk Management
Location: Noida, India | Category: Consulting | Employment Type: Full-Time | Job ID: R2693 | Posted: January 9, 2026

About Cencora
Cencora is a leading global healthcare organization dedicated to improving the lives of people and animals worldwide. Our team members are essential to delivering innovative healthcare solutions and maintaining the highest standards of safety, compliance, and quality.

Role Overview
We are seeking a Specialist in Pharmacovigilance (PV) Epidemiology & Risk Management to support safety monitoring, risk assessment, and regulatory compliance. This position provides hands-on experience in Individual Case Safety Report (ICSR) management, quality assurance, and mentoring new team members. The role is based in Noida, India, and offers exposure to global pharmacovigilance operations.

Key Responsibilities

  • Perform triage and initial validity assessments for cases, including spontaneous reports, clinical trials, literature, and health authority submissions.

  • Enter and maintain case data in PV databases.

  • Conduct initial ICSR assessments and determine the need for expedited reporting to Health Authorities and client partners.

  • Prepare and submit standard reporting forms (e.g., CIOMS I, MedWatch, XML files).

  • Send follow-up requests and complete case documentation in compliance with regulatory standards.

  • Conduct quality checks of ICSRs to ensure adherence to project requirements and best practices, maintaining integrity and reliability of safety data.

  • Search, retrieve, and assess ICSRs from the EVWEB database for company and non-company cases.

  • Mentor and guide new team members, supporting their integration and professional development.

  • Perform additional responsibilities as assigned by supervisors in alignment with process requirements.

Qualification & Skills

  • University degree in Life Sciences.

  • Basic experience in pharmacovigilance or related field; willingness to learn on-the-job.

  • Strong attention to detail and high service orientation.

  • Ability to prioritize tasks, manage time efficiently, and work independently.

  • Excellent written and verbal communication skills, with the ability to identify issues and propose solutions.

  • Professional appearance and business fluency in English.

What Cencora Offers

  • Competitive compensation and benefits aligned with local market practices.

  • Opportunities for professional development in a global healthcare environment.

  • Supportive and inclusive workplace culture that values safety, innovation, and collaboration.

Equal Employment Opportunity
Cencora is committed to providing equal employment opportunities without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or other legally protected categories. Reasonable accommodations are available for individuals with disabilities during the employment process.

Affiliated Company: PharmaLex India Private Limited

Application Information
Interested candidates can apply through the company portal. For accommodation requests, contact hrsc@cencora.com or call 888.692.2272.