Freelance / Consultant 0.5 FTE Local Contact Person for Pharmacovigilance and Regulatory Affair[...]
hace 5 días
Company DescriptionWe are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance.PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device.Job DescriptionThis is an exciting opportunity for a freelancer / consultant to join our team as Local Contact Person for Pharmacovigilance and Regulatory Affairs at 0.5 FTE.By working with us, you will have the opportunity to work in an international team and strengthen your expertise within the broad and diverse PV and Regulatory Affairs area.Main ResponsibilitiesPrimary contact person for local regulatory authority / Pharmacovigilance expert as per local requirementsPrompt and effective communication with local regulatory authoritiesProvision of local regulatory intelligence screening and expert adviceCollection and reporting of locally suspected ADRs or ICSRs (FUs, translations)Local management / oversight of risk minimization measures related to urgent safety restrictions and emerging safety issuesReview and linguistic input on local Product Information and Mock-upsPerform local non-indexed literature screening and screening of Regulatory Authority website/s for potential Adverse Drug Reactions (ADRs) and safety informationSupport audits and InspectionsHandle local QA tasks such as suspected falsified products, quality alerts received from HA and other quality-related requirements received from the local marketQualificationsBachelor's Degree in Life Sciences or Chemistry, Nursing or equivalent experienceDemonstrated experience within pharmaceutical or CRO industry or Regulatory bodyMust have experience within LCPPV / LCPRA rolesPV training and/or working experience and other educational or professional background as required locallyExpert knowledge of ICH GVP and most relevant legislation/local requirements for territories of competencyProficiency in English, both written and verbal and in local languageProficiency in all MS-Office applications including Microsoft Word, Excel, and PowerPointMust currently be set up to work as a freelancer / consultantAdditional InformationWe prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.To succeed we must work together with a human first approach. Why? Because our people are our greatest strength leading to our continued success on improving the lives of those around us.Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to joinQualityIntegrity & TrustDrive & PassionAgility & ResponsivenessBelongingCollaborative PartnershipsWe look forward to welcoming your application.
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