
10.000+ Mitarbeiter
Gegründet 1849
💼 Beratung
📣 Marketing
💊 Pharmazie
💰 Post-IPO Debt im 2023-05
Consulting • Marketing • Pharmaceuticals
Wir feiern 175 Jahre mutige wissenschaftliche Innovation – und wir sind noch nicht am Ende. Jeden Tag lenken wir unsere Leidenschaft und Ressourcen darauf, innovative Therapien zu entwickeln, die das Gesicht des Gesundheitswesens verändern. Lassen Sie uns den gestrigen Tag übertreffen.
🕒 vor 26 Tagen
🗣️🇺🇸🇬🇧 Englisch erforderlich
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10.000+ Mitarbeiter
Gegründet 1849
💼 Beratung
📣 Marketing
💊 Pharmazie
💰 Post-IPO Debt im 2023-05
Consulting • Marketing • Pharmaceuticals
Wir feiern 175 Jahre mutige wissenschaftliche Innovation – und wir sind noch nicht am Ende. Jeden Tag lenken wir unsere Leidenschaft und Ressourcen darauf, innovative Therapien zu entwickeln, die das Gesicht des Gesundheitswesens verändern. Lassen Sie uns den gestrigen Tag übertreffen.
• Provide medical and scientific information on Pfizer Biopharmaceutical Group products to internal and external customers in compliance with procedures and regulations • Collaborate with Drug Safety, Global/Regional Therapeutic Areas and Regulatory Affairs on risk management plans and safety studies • Review and assess local-language product documents • Manage clinical and research collaborations and local/regional interventional and non-interventional studies • Advise commercial colleagues on compliance and serve as the medical spokesperson to healthcare authorities • Coach MSLs and maintain relationships with KOLs, medical societies and academic centers • Manage the Medical Affairs annual budget and local plan • Lead locally sponsored clinical trials, including investigator selection, site identification, investigator meetings, timelines, budgets and registry updates • Manage compassionate access programs and ensure adherence to Pfizer requirements and local regulations • Lead publication strategies and participate in audits, inspections and CAPA implementation • Provide medical and scientific input for product setup, launches, strategic planning, marketing campaigns and promotional materials • Review and validate scientific content, training materials and product information • Coordinate scientific events, advisory boards, speaker training and medical education programs • Train commercial colleagues and trainers on product and disease knowledge • Support market research, Corporate Affairs communications, business meetings and medical training • Author or review medical papers • Conduct periodic field visits with physicians • Review and approve local product documents and package inserts • Support product registration and preparation of regulatory-authority meetings • Prepare medical and scientific information for formularies, listings and regulatory dossiers • Follow up on adverse events and support Medical Information dossiers and promotional materials • Complete required training and participate in inspection-readiness activities
• Fluency in English (both written and spoken) • Ability to prepare presentations and deliver public speeches • Ability to teach and train • Abilities in negotiation and effective communication • Excellent abilities in strategic and interpersonal influence • Knowledge of scientific, ethical, regulatory and legal aspects which allow the conduction of research trials in human beings • Ability to handle computer software, specifically Microsoft Office, internet and other basic electronic tools • Business and financial acumen, including budget management • Minimum of 3 years’ experience in positions within clinical practice or linked with medical affairs, R&D, medical-marketing, marketing, clinical research or medical direction, preferably within the pharmaceutical industry • Medical knowledge in the assigned medical area of the products entrusted • Medical degree required, preferably specialty • Experience in project and budget administration and management • Technically updated in local regulations
• Equal opportunity in the terms and conditions of employment • Business travel
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