Senior Pv Associate

Benefits Exceptional learning and development opportunitiesBe a key player at a global headquarters with a strong local presenceHybrid working model – 3 days in the Sydney office, 2 days remoteAbout the Opportunity In this role you will:
Serve as the subject matter expert in Pharmacovigilance, expanding your expertise across various therapeutic areas and product categoriesTake a proactive leadership role within a global headquarters for local brandsAct as the Deputy QPPVManage adverse event and safety data to ensure regulatory complianceLead efforts to continuously improve PV and Quality Management SystemsDevelop and deliver PV-related training programsProvide oversight on Organised Data Collection SystemsCollaborate effectively with internal and external stakeholdersAssist in the preparation and submission of PSUR, ASA, and RMP documentsSkills and Experience A tertiary degree in Pharmacy, Biomedical Science, Nursing, or a related healthcare field2-3 years of experience in PharmacovigilanceA quick learner with a passion for professional growthSolid understanding of pharmacovigilance regulations and guidelines, including TGA, Medsafe, and ACCCProven experience in audits, inspections, and the development of PV proceduresProficiency in using tracking tools and systemsExperience with the ARGUS database and MedDRA codingCulture This company's values—Commitment, Excellence, Innovation, Integrity, and Teamwork—are at the heart of everything they do. If you are driven by these principles and eager to contribute to a meaningful mission in healthcare, we want to hear from you.
How to Apply Click 'Apply' or contact Davina Ocansey, Senior Recruitment Consultant, at +61 2 8877 8712 for a confidential discussion.

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