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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: R2519675 | Posted: January 4, 2026

About Cencora
Cencora is a leading global healthcare organization committed to improving the lives of people and animals worldwide. Our team members are central to our mission, enabling us to deliver innovative healthcare solutions while maintaining the highest standards of quality and safety.

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

Key Responsibilities

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

  • Enter and manage 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).

  • Prepare and send follow-up requests for additional information when required.

  • Ensure timely submission of ICSRs to Health Authorities and partners.

  • Complete case documentation and maintain high-quality standards.

  • Conduct quality checks of ICSRs to ensure compliance with project requirements, industry standards, and regulatory guidelines.

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

  • Mentor and guide new joiners, facilitating their integration and supporting professional development.

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

Required Qualifications & Experience

  • Bachelor’s degree in pharmacy, life sciences, or a related field.

  • Hands-on experience in pharmacovigilance case processing and ICSR management.

  • Knowledge of regulatory requirements and best practices in safety reporting.

  • Strong analytical, problem-solving, and attention-to-detail skills.

  • Effective communication skills and ability to work collaboratively in cross-functional teams.

  • Experience mentoring or supporting team members is a plus.

What Cencora Offers

  • Competitive compensation and benefits aligned with local market practices.

  • Opportunities for professional growth and 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.