14.01.2025 | Full-time | PrimeVigilanceRecord of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs Strong PV Project Management experience from ideally a service provider - CRO Health Care
Uita-te mai târziu14.01.2025 | Full-time | PrimeVigilanceData and ensures accuracy Is involved in ICSR processing and 2nd QC of cases Support other departments, as approved and instructed by ICSR Operational Lead Qualifications Life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance Strong previous
Uita-te mai târziu10.01.2025 | Full-time | PrimeVigilanceDrug safety. The PV Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trial, to large, generic post
Uita-te mai târziu10.01.2025 | Full-time | PrimeVigilanceJob Description POSITION SUMMARY Manages ICSR Management Unit for assigned staff and ensures all unit-relevant activities are delivered within agreed extent. Contributes to achieving company´s goals and objectives. Performs project budget reviews, and provides support to, and management of, the ICS
Uita-te mai târziu11.01.2025 | Full-time | PrimeVigilanceDocuments for medical writing, including internal templates and formats required for standardised documentation Support in all pharmacovigilance operations associated with medical writing Continuous self-education in all aspects associated with medical writing Managing a team of junior medical writers
Uita-te mai târziu31.12.2024 | Full-time | ParexelAnd involvement in Pharmacovigilance/Drug Safety. This is a newly created role for the EMEA region and requires previous team management experience along with the potential and desire to grow into a bigger leadership Purpose The Senior Medical Director is responsible for providing leadership
Uita-te mai târziu25.10.2024 | Full-time | Teva PharmaceuticalsThe opportunityAs a Director, Pharmacovigilance Safety Physician you will lead activities necessary for the determination of the safety profile and the characterization, monitoring, and mitigation of risk for the assigned products throughout the product lifecycle and provide comprehensive safety
Uita-te mai târziu17.10.2024 | Full-time | Teva PharmaceuticalsThe opportunityAs an Associate Director, Pharmacovigilance Safety Physician you will conduct activities necessary for the determination of the safety profile and the characterization, monitoring, and mitigation of risk for the assigned products throughout the product lifecycle and provide
Uita-te mai târziu28.06.2024 | Full-time | Worldwide Clinical TrialsRequisition Number7970Employment TypeRegularWho we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to
Uita-te mai târziu10.01.2025 | Full-time | PrimeVigilanceBiology, biotechnology, veterinary science etc.) and have demonstrated experience in case processing. The PV Officer will be working as part of a project team, performing, and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Responsibilities include Processing of Individual
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