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Showing posts with the label Drug Safety Careers 2025

iCRO Hiring Freshers for Pharmacovigilance Associate | B.Pharm, M.Pharm & Life Sciences | JLPT N2 Required

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iCRO Hiring Freshers for Pharmacovigilance Associate | B.Pharm, M.Pharm & Life Sciences Candidates Can Apply (iCRO Hiring Freshers for Pharmacovigilance Associate) Introduction If you are a Pharmacy or Life Sciences graduate with Japanese language proficiency and are looking to start a career in the pharmaceutical industry, this opportunity may be worth exploring. iCRO has announced Pharmacovigilance Associate openings for freshers, offering exposure to global drug safety operations, adverse event reporting, literature review, regulatory documentation, and international pharmacovigilance projects. This role is particularly attractive for candidates who possess JLPT N2 or higher Japanese language certification and wish to combine their scientific knowledge with international healthcare and pharmaceutical operations. Selected candidates may also receive opportunities for global training, client interactions, and future overseas assignments depending on business requirements. ...

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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"

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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now" (ProPharma Hiring Pharmacovigilance) Are you passionate about drug safety and pharmacovigilance ? ProPharma, a trusted global leader in regulatory sciences, clinical research, and drug safety , is inviting applications for the  Pharmacovigilance Safety Scientist  role in India. This position offers an excellent opportunity to work on global projects and contribute to improving patient safety worldwide. Key Responsibilities:- As a Pharmacovigilance Safety Scientist at ProPharma , you will be responsible for: Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR . Developing and maintaining Risk Management Plans (RMPs) . Preparing Signal Management Reports and conducting literature searches. Reconciling process trackers and validating extracted data. Generating and reviewing line listings from safety databases . Supporting ad-hoc pharmacovigilance acti...

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