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Trainee- Specialist, Pharmacovigilance, Epidemiology & Risk Management

Cencora
Cencora
0-2 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

Trainee / Specialist – Pharmacovigilance, Epidemiology & Risk Management

Location: Noida, India
Employment Type: Full-Time
Experience Required: Freshers / 0–2 Years in Pharmacovigilance or Life Sciences
Job ID: R2523626
Category: Consulting / Life Sciences


About Cencora

Cencora is a leading healthcare company dedicated to creating healthier futures for people and animals worldwide. Our mission is centered on improving lives through innovation, scientific excellence, and patient-focused solutions. Every team member is valued, empowered, and plays a key role in delivering our purpose. If you are passionate about contributing to global health and making a meaningful impact, Cencora is the place for you.


Job Summary

As a Trainee / Specialist in Pharmacovigilance, Epidemiology & Risk Management, you will support critical drug safety and regulatory reporting activities. You will gain hands-on experience in adverse event reporting, case evaluation, and regulatory compliance, working within a collaborative, high-performing team.

This role is ideal for B. Pharma, M. Pharma, BDS, or Life Sciences graduates seeking to start or grow their career in pharmacovigilance and risk management.


Key Responsibilities

  • Conduct triage and initial validity assessments of adverse event cases from multiple sources, including spontaneous reports, clinical trials, health authority notifications, and published literature

  • Enter data accurately and efficiently into pharmacovigilance databases

  • Perform initial Individual Case Safety Report (ICSR) assessments in compliance with regulatory requirements

  • Evaluate cases for expedited reporting obligations to health authorities and client partners, ensuring adherence to timelines

  • Prepare standardized regulatory reporting forms, including CIOMS I forms, MedWatch forms, and XML formats

  • Develop and follow-up on requests for additional case information as required

  • Maintain thorough and compliant case documentation to meet quality and regulatory standards

  • Conduct ICSR searches and retrievals from databases such as EVWEB

  • Support additional pharmacovigilance and risk management activities as assigned


Required Qualifications

  • Education: B. Pharma, M. Pharma, BDS, or Life Science Graduate

  • Experience: Freshers or up to 2 years of experience in pharmacovigilance or related fields

  • Familiarity with pharmacovigilance processes, regulatory reporting standards, and ICSR documentation (preferred)

  • Excellent communication and interpersonal skills

  • Strong attention to detail and ability to work under regulatory timelines


Why Join Cencora

  • Opportunity to launch a career in global pharmacovigilance and risk management

  • Exposure to regulatory reporting, epidemiology, and drug safety operations

  • Structured training and mentorship to develop professional skills and industry expertise

  • Inclusive and supportive workplace committed to career growth and learning

  • Equal Opportunity Employer: Cencora provides fair hiring practices and reasonable accommodations for individuals with disabilities


Apply now on ThePharmaDaily.com to start your career in Pharmacovigilance and Risk Management with a globally recognized healthcare company.