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Pharmacovigilance Associate

0.00 to 1.00 Years   Mumbai City,Pune, Bangalore, Hyderabad   01 Apr, 2025
CLIN BIOSCIENCES
Job LocationMumbai City,Pune, Bangalore, Hyderabad
EducationNot Mentioned
SalaryRs 4.5 - 7 Lakh/Yr
IndustryPharma / Biotech
Functional AreaBio Tech / R&D / ScientistPharmacist / Medical Representative
EmploymentTypeFull-time

Job Description

    Roles and Responsibilities
    • Adverse event collection and reporting: Receiving and reviewing adverse event reports from healthcare professionals, clinical trials, and other sources.
    • Case processing: Performing detailed analysis of adverse events, including medical coding using MedDRA (Medical Dictionary for Regulatory Activities) to accurately categorize and classify the events.
    • Signal detection: Identifying potential safety signals by analyzing patterns in adverse event data, including trends and clusters. Risk assessment: Evaluating the severity and causality of adverse events to determine the potential risk associated with a drug.
    • Regulatory reporting: Preparing and submitting timely reports to regulatory agencies regarding serious adverse events and safety concerns.
    • Literature review: Monitoring published medical literature for potential safety concerns related to the drug.
    • Collaborating with cross-functional teams: Working with clinical researchers, medical affairs, and marketing teams to communicate safety information and address potential safety issues.
    Qualifications
    • Bachelors degree in a related field, such as pharmacy, nursing, or biology
    • 0-2 years of experience in pharmacovigilance or a related field
    • Strong analytical and problem-solving skills
    • Excellent communication and interpersonal skills
    • Ability to work independently and as part of a team
    Interested to apply can share CV or call/whatsapp tohidden_mobile

Keyskills :
argus safetyarisgdrug safety

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