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    Cencora Trainee Pharmacovigilance Specialist Job in Noida – Apply Now

    Cencora Trainee Opportunity | Start Your Career in Pharmacovigilance Jobs & Risk Management Jobs

    Begin your professional journey with one of the best Pharmacovigilance jobs available today through Cencora, where you also gain strong exposure to Risk management jobs in global drug safety, epidemiology, and regulatory compliance. This Noida-based trainee role offers unmatched learning, hands-on ICSR handling, and real-world safety monitoring experience with an industry-leading healthcare organization.

    Job Details

    • Position: Trainee- Specialist, Pharmacovigilance, Epidemiology & Risk Management
    • Location: Noida, India
    • Job ID: R2523626

    About the Company

    Cencora is a global healthcare leader creating healthier futures worldwide. The organization empowers professionals to thrive in Pharmacovigilance jobs and Risk management jobs, ensuring patient safety, regulatory excellence, and innovation in life sciences. This role is affiliated with PharmaLex India Private Limited.

    Job Description

    The Trainee – Specialist Pharmacovigilance, Epidemiology & Risk Management position focuses on adverse event case processing, epidemiology activities, ICSR assessments, compliance documentation, and execution of safety reporting aligned with global regulatory expectations.

    Key Responsibilities | Pharmacovigilance Jobs

    • 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.

    Qualifications required for Pharmacovigilance Jobs

    • B. Pharma, M. Pharma Graduate

    Skills:

    • Excellent communication skill
    • Attention to detail and ability to work under regulatory timelines
    • Familiarity with pharmacovigilance processes and reporting standards (preferred)

    CLICK HERE TO APPLY ONLINE

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