Lavori attuali relativi a Lead Coordinator, Professional Affairs... - Lazio - Powertofly
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Lazio, Italia Jobbit A tempo pienoRegulatory Affairs Coordinator Central and Latin America Regulatory Affairs Coordinator Central and Latin America role for a pharmaceutical client in Florence, Italy.The Global Regulatory Affairs Department seeks a dedicated, detail-oriented regulatory professional to ensure compliance across diverse markets and support timely...
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Regulatory Affairs Head Italy — Submissions
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Lazio, Italia Merck Healthcare A tempo pienoA global pharmaceutical leader is seeking a Regulatory Affairs Head in Italy to lead a team of Regulatory professionals.The successful candidate will manage local submissions, define engagement strategies with health authorities, and ensure compliance with regulations.The role requires a pharmacy degree, extensive experience in Regulatory Affairs, and strong...
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Professional Affairs Consultant
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Lazio, Italia Michael Page International Italia S.R.L. A tempo pienoProfessional Affairs ConsultantImportante multinazionale settore oftalmico, contesto dinamico e innovativo.AziendaL'azienda è una grande organizzazione che opera nel settore oftalmico.Si impegna a fornire soluzioni di alta qualità per migliorare la salute e il benessere delle persone.OffertaFormazione tecnica e scientifica rivolta ai professionisti del...
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Lead Coordinator, Professional Affairs...
4 minuti fa
Lazio, Italia Powertofly A tempo pienoEnsure communication with PA team and Marketing / EventsMaintain understanding of relevant regulations and laws, including MedTech CodeCollaborate in process improvement projectsRegular review of processes to ensure updates to any regulations, compliance policies are updatedRegular meetings with the Manager and PA Team to ensure workload is even and capacity...
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Medical Affairs Lead
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Lazio, Italia Clinigen A tempo pienoRole Description In this role, you will be responsible for establishing and maintaining strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the medical community.You will play a pivotal role in supporting the company's medical strategy and ensuring the accurate and ethical dissemination of medical...
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Senior Medical Affairs Lead, Gi
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Lazio, Italia Ali Professional A tempo pienoAli Professional ricerca per importante realtà internazionale del settore chimico-farmaceutico un/una: Regulatory Affairs SpecialistLa risorsa sarà inserita nel dipartimento Regulatory Affairs e sarà responsabile della gestione delle attività normative relative ai prodotti di propria competenza, assicurando la conformità alle procedure aziendali e alla...
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Gi/Inflammation Medical Affairs Lead
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Lazio, Italia Tmc A tempo pienoA leading pharmaceutical company in Rome is seeking a Medical Affairs Specialist with expertise in the Gastrointestinal/Injury Therapeutic Area.The role includes developing medical strategies, engaging with key stakeholders, and ensuring compliance with regulatory standards.Ideal candidates will have a medical degree and over 3 years of experience in medical...
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Market Access
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Lazio, Italia Pharma Point A tempo pienoMarket Access & Government Affairs Director ItalyThe OpportunityOur client is a mid-sized specialty biopharma focused exclusively on high-value, specialist-driven therapeutic areas.With multiple launches planned, we are hiring a Market Access & Government Affairs Director to lead Italy market access and external affairs.This is a high-impact role combining...
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Market Access
4 ore fa
Lazio, Italia Pharma Point A tempo pienoMarket Access & Government Affairs Director Italy The Opportunity Our client is a mid-sized specialty biopharma focused exclusively on high-value, specialist-driven therapeutic areas. With multiple launches planned, we are hiring a Market Access & Government Affairs Director to lead Italy market access and external affairs. This is a high-impact role...
Lead Coordinator, Professional Affairs...
3 ore fa
What you will do - Ensure communication with PA team and Marketing/Events- Maintain understanding of relevant regulations and laws, including MedTech Code- Collaborate in process improvement projects- Regular review of processes to ensure updates to any regulations, compliance policies are updated- Regular meetings with the Manager and PA Team to ensure workload is even and capacity used effectively- CNF Consultant Profile creation in the compliance tool for Southern EU PA - All Divisions- Collaboration for HCP Contract Process in creating the Contract Form for all SE contracts all Divisions- Faculty Service invoices paying process and vendors creations management working with the SE PA Team, Invoicing Team for all consultants all divisions Southern Europe- Interacting and advising business units on compliant HCP Consultant activitiesWhat you needEducation- Essential: College equivalent qualifications- Desired: Bachelor's Degree desired but not essentialExperience- Essential: New graduate or 1-2 years relevant experience- Desirable: Fluent and skilled in local language as well as Spanish and English- Desirable: Work experience in a Medical Device/Pharmaceutical company- Desirable: Knowledge of MedTech Europe Compliance- Desirable: Sound excel knowledgeCompetencies & Behaviors- Highly organized- Ability to multitask- Processed focused- Strong interpersonal Skills- Strong communication skills (written & verbal) at all levels- Ability to manage professional relationships with both internal and external stakeholders- Hard working and flexiblePay rate will not be below any applicable local minimum wage rates.Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better.The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes.Alongside its customers around the world, Stryker impacts more than 150 million patients annually.#J-*****-Ljbffr
