Cencora Careers: Apply Now for Trainee Position
Cencora Careers: Cencora is hiring a Trainee – Specialist, Pharmacovigilance, Epidemiology & Risk Management to join its consulting team in Noida, India. This full-time opportunity is ideal for medical science graduates looking to build a strong foundation in global drug safety and regulatory compliance. Explore this role through Cencora Careers and be part of an organization committed to creating healthier futures worldwide.
Cencora Careers: Job Details
- Job Title: Trainee – Specialist, Pharmacovigilance, Epidemiology & Risk Management
- Job ID: R2523626
- Category: Consulting
- Job Location: Noida, India
- Employment Type: Full-Time
About Cencora
Cencora is a global healthcare company focused on improving lives across the pharmaceutical, biotech, and healthcare ecosystems. Driven by innovation and purpose, Cencora supports patients, healthcare professionals, and partners by delivering trusted solutions at the center of health.
Cencora Careers: Educational Qualifications
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BDS graduate from a recognized institute.
About the Role
The trainee specialist will support pharmacovigilance and risk management activities, ensuring accurate safety data processing and regulatory compliance across global reporting systems.
Key Responsibilities
- Conduct triage and initial validity assessments of adverse event cases from multiple sources, including spontaneous reports, health authority notifications, clinical trials, and published literature
- Perform accurate and timely data entry into pharmacovigilance databases
- Complete initial Individual Case Safety Report (ICSR) assessments in accordance with regulatory requirements
- Evaluate case criteria to determine expedited reporting obligations to Health Authorities and client partners, ensuring compliance with applicable reporting timelines
- Prepare standardized regulatory reporting forms, including CIOMS I form, MedWatch forms, and XML file formats
- Develop and transmit follow-up requests to obtain additional case information as needed
- Ensure thorough case documentation and completion in compliance with quality standards
- Conduct ICSR searches and retrieval from the EVWEB database, performing company/non-company assessments for case processing
- Undertake additional responsibilities as assigned by the supervisor based on operational and process requirements.
Required Skills
- Excellent communication skills
- Strong attention to detail and ability to meet regulatory timelines
- Familiarity with pharmacovigilance processes (preferred)
Why Join Cencora?
- Exposure to global pharmacovigilance operations
- Structured learning and career development
- Inclusive, ethical, and purpose-driven work culture
- Opportunity to work at the center of healthcare innovation
