Aktuelle Jobs im Zusammenhang mit Head of Medical Affairs Europe - Opfikon - CSL Behring
-
Global Head of Medical Evidence Generation
vor 3 Monaten
Opfikon, Schweiz CSL Vifor Vollzeit**The Opportunity** We are looking for a Global Head of Medical Evidence Generation to join our patientfocused team in Zurich, Switzerland. Reporting to the VP, Global Head of Medical Affairs at CSL Vifor, you will have a pivotal role in shaping evidence generation across the organization. **Main Accountabilities** - Define the overarching RWE strategy...
-
Global Head of Medical Evidence Generation
vor 1 Monat
Opfikon, Zürich, Schweiz CSL Vifor VollzeitGlobal Head of Medical Evidence GenerationAbout the RoleWe are seeking a highly skilled and experienced professional to lead our Medical Evidence Generation team. As the Global Head of Medical Evidence Generation, you will be responsible for developing and implementing strategies to generate high-quality medical evidence to support our products and...
-
Global Head of Medical Evidence Generation
vor 4 Wochen
Opfikon, Zürich, Schweiz CSL Vifor VollzeitGlobal Head of Medical Evidence GenerationAbout the RoleWe are seeking a highly skilled and experienced professional to lead our Medical Evidence Generation team. As the Global Head of Medical Evidence Generation, you will be responsible for developing and implementing strategies to generate high-quality medical evidence to support our products and...
-
Global Head of Medical Evidence Generation
vor 1 Monat
Opfikon, Zürich, Schweiz CSL Vifor VollzeitMain ResponsibilitiesThe Global Head of Medical Evidence Generation will play a pivotal role in shaping evidence generation across CSL Vifor. Reporting to the VP, Global Head of Medical Affairs, this individual will define the overarching RWE strategy across the portfolio, aligning with overall evidence generation activities and translating data to insights...
-
Global Head of Medical Evidence Generation
vor 3 Wochen
Opfikon, Zürich, Schweiz CSL Vifor VollzeitGlobal Head of Medical Evidence GenerationAbout the RoleCSL Vifor is seeking a highly skilled and experienced Global Head of Medical Evidence Generation to join our team in Zurich, Switzerland. As a key member of our Medical Affairs department, you will be responsible for leading the development and implementation of evidence generation strategies across the...
-
Global Head of Medical Evidence Generation
vor 2 Monaten
Opfikon, Zürich, Schweiz CSL Vifor VollzeitGlobal Head of Medical Evidence GenerationAbout the RoleWe are seeking a highly skilled and experienced Global Head of Medical Evidence Generation to join our team at CSL Vifor. As a key member of our Medical Affairs department, you will play a pivotal role in shaping our evidence generation strategy across the organization.Main ResponsibilitiesDevelop and...
-
Global Head of Medical Evidence Generation
vor 3 Monaten
Opfikon, Schweiz CSL Vifor VollzeitThe Opportunity We are looking for a Global Head of Medical Evidence Generation to join our patientfocused team in Zurich, Switzerland. Reporting to the VP, Global Head of Medical Affairs at CSL Vifor, you will have a pivotal role in shaping evidence generation across the organization.Main AccountabilitiesDefine the overarching RWE strategy across the...
-
Global Head of Medical Evidence Generation
vor 3 Monaten
Opfikon, Schweiz CSL Vifor VollzeitThe Opportunity We are looking for a Global Head of Medical Evidence Generation to join our patientfocused team in Zurich, Switzerland. Reporting to the VP, Global Head of Medical Affairs at CSL Vifor, you will have a pivotal role in shaping evidence generation across the organization.Main AccountabilitiesDefine the overarching RWE strategy across the...
-
Global Head of Medical Evidence Generation
vor 1 Monat
Opfikon, Zürich, Schweiz CSL Vifor VollzeitGlobal Head of Medical Evidence Generation OpportunityWe are seeking a highly skilled and experienced professional to lead our Medical Evidence Generation team as Global Head. This role will play a pivotal part in shaping our evidence generation strategy across the organization, ensuring alignment with overall evidence generation activities, and translating...
-
Global Head of Medical Evidence Generation and Strategy
vor 2 Monaten
Opfikon, Zürich, Schweiz CSL Vifor VollzeitAbout the RoleWe are seeking a highly skilled and experienced professional to lead our Medical Evidence Generation and Strategy team at CSL Vifor. As the Global Head of Medical Evidence Generation and Strategy, you will play a pivotal role in shaping our evidence generation activities across the organization.Key ResponsibilitiesDevelop and Implement Evidence...
-
Regional Regulatory Affairs Specialist
vor 2 Monaten
Opfikon, Zürich, Schweiz CSL VollzeitJob Purpose:We are seeking an experienced Regulatory Affairs professional to lead our Cardio-Renal Therapeutic Area in the Intercontinental Region. As a key member of our Global Regulatory Affairs team, you will develop regional strategies, contribute to global regulatory strategies, and submit regulatory applications to obtain Health Authority approval in...
-
Regional Regulatory Affairs Manager
vor 1 Monat
Opfikon, Zürich, Schweiz CSL VollzeitJob Purpose:We are seeking an experienced and skilled Regulatory Affairs professional to lead the Cardio-Renal Therapeutic Area in the Intercontinental Region. As a key member of the Global Regulatory Affairs team, you will develop regional strategies, contribute to global regulatory strategies, and submit regulatory applications to obtain Health Authority...
-
Senior Regulatory Affairs Specialist
Vor 6 Tagen
Opfikon, Zürich, Schweiz CSL VollzeitJob Purpose:CSL is seeking a highly experienced and skilled Regulatory Affairs Specialist to lead the development of regional strategies in the Cardio-Renal Therapeutic Area. This individual will contribute to global regulatory strategies and submit regulatory applications for development products and change applications for registered products to obtain...
-
Regional Regulatory Affairs Specialist
vor 1 Woche
Opfikon, Zürich, Schweiz CSL VollzeitJob Purpose:We are seeking a highly experienced Regulatory Affairs Specialist to lead the development of regional strategies and contribute to global regulatory strategies for the Cardio-Renal Therapeutic Area in the Intercontinental Region. You will be responsible for submitting regulatory applications for development products and change applications for...
-
Director of Global Regulatory Affairs Operations
vor 2 Wochen
Opfikon, Zürich, Schweiz CSL Vifor VollzeitJob SummaryWe are seeking a highly experienced and skilled Director of Global Regulatory Affairs Operations to join our team at CSL Vifor. As a key member of our Global Regulatory Affairs department, you will be responsible for leading the Central Services Group (CSG) team, which is pivotal in shaping our ability to deliver efficient and timely worldwide...
-
Medical Information Manager
vor 5 Monaten
Glattpark (Opfikon), Schweiz Panda International Vollzeit**Medical Information Manager**: **Location** - Glattpark-Opfikon,, Switzerland **Business Sector** - Biotechnology **Job ref** - 22899 **Published** - 2 minutes ago **Medical Information Manager** For my client - a globally renowned biotech in Zurich, Switzerland - I am looking for an experience Medical Information Manager join an innovative and...
-
Director of Global Regulatory Affairs Operations
vor 1 Monat
Opfikon, Zürich, Schweiz CSL Vifor VollzeitJob Title: Director of Global Regulatory Affairs OperationsCSL Vifor is a global biotechnology company with a dynamic portfolio of lifesaving medicines. We are seeking a highly skilled Director of Global Regulatory Affairs Operations to join our team.The successful candidate will be responsible for leading the global Central Services Group (CSG) team, which...
-
Director of Global Regulatory Affairs Operations
vor 1 Woche
Opfikon, Zürich, Schweiz CSL Vifor VollzeitCSL Vifor is a global biotechnology company with a dynamic portfolio of lifesaving medicines. As the Director of Global Regulatory Affairs Operations, you will play a pivotal role in shaping the company's ability to deliver efficiently and timely our worldwide submissions.The Global Regulatory Affairs Operations team is responsible for prioritizing,...
-
Director of Global Regulatory Affairs Operations
vor 2 Wochen
Opfikon, Zürich, Schweiz CSL Vifor VollzeitJob SummaryCSL Vifor is seeking a highly skilled and experienced professional to lead our Central Services Group (CSG). As the Director of Global Regulatory Affairs Operations, you will be responsible for building and managing a global team that prioritizes, plans, prepares, and coordinates all submissions related to our product portfolio.Key...
-
Head of Fp&a
vor 5 Monaten
Opfikon, Schweiz General Motors Vollzeit**Job Description**: **Who We Look For** **We look for the bold**: - those willing to respectfully share their ideas and listen to others. **We seek out the innovators**: - those who challenge the status quo when their vision requires a new way of thinking. **We reach for the collaborators**: - those who understand that a diverse team is stronger than...
Head of Medical Affairs Europe
vor 3 Monaten
Main Accountabilities
- Direct Reporting Line : As we transition reporting lines from the Country General Managers to the incumbent of this role, you will establish a robust and accountable solid reporting line for all European Country Medical Directors. Ensuring clear oversight and yet guaranteeing their close collaboration with the GMs, as they will continue to be part of the local LT and supporting local success. This role reports into the VP Head of Global Medical Affairs.
- Governance and Oversight : Take ownership for governance oversight of Medical Affairs activities across Europe (and beyond where applicable). Drive the regular Medical Directors Forum for Europe, which informs the yearly Global Medical Affairs Directors Meeting. Member of European Leadership Team and Global Medical Affairs Leadership Team (GMA LT).
- Strategic Alignment : Align strategic objectives and by country priorities with cross-functional regional team Europe as well as with the Global Medical Affairs team / Global Brand Teams.
- Initiative Development : Lead the development and execution of diverse Medical Affairs initiatives. Serve as the primary point of contact and provide day-to-day support to Country Medical Directors in managing their medical teams.
- Representation and Leadership : Advocate for European interests with Global Medical Excellence, Global Medical Affairs and Global Brand Teams. Assume a strategic leadership role across CSL Vifor.
- Collaboration and Insight : Collaborate closely with commercial, market access, and marketing functions. Offer forward-thinking medical insights related to therapeutic areas within the Vifor Pharma portfolio.
- Capability Building : Continuously enhance the capabilities of the Medical Affairs team, leveraging support from the Global Medical Excellence and Governance organization.
- Leadership : Exhibit excellent medical leadership, contributing to the development and effective management of Medical Affairs in Europe and beyond.
Key Measures of Success
- Strategic Impact : Develop and execute the Global/Regional Medical Affairs strategy and programs, driving successful commercialization of in-market and future CSL Vifor products. Emphasize evidence-based medicine and value-based pricing.
- Leadership Recognition : Establish yourself as a recognized medical leader both internally and externally. Demonstrate strong leadership qualities, foster cross-functional collaboration, and influence stakeholders at all organizational levels.
- Collaboration Alignment : Act as a collaborative internal partner to Global Medical Affairs (GMA), ensuring regional needs inform an overarching GMA strategy.
- Global Influence : Strengthen collaborations with global functions to proactively shape clinical development plans that align with the region’s growth ambitions.
- Technical Consultation : Provide continuous technical and scientific consultation to both the medical and commercial teams, ensuring adherence to quality and compliance systems.
- Medical Compliance : Ensure all activities adhere to regulatory and legal frameworks, including GCP, IFPMA, local regulations, and CSL Vifor policies and healthcare compliance procedures.
Tasks
- Provide insights to identify area for research interest for independent research : Inform the global Investigator-Initiated Trial (IIT) strategy per molecule by means of identified evidence gaps. Support company-sponsored post-marketing clinical trials across the region, ensuring alignment with our evidence gaps and the Global Medical Affairs Strategy.
- Brand Value Maximization : Collaborate with Marketing Teams to maximize the brand value proposition in assigned therapeutic areas. Contribute to the development and execution of Medical Marketing plans and commercial activities.
- Scientific Support : Provide scientific support to Marketing, Regulatory, Market Access, Pharmacovigilance, and Compliance (risk management) groups.
- International Management Strategy : Work closely with Global Medical Affairs (GMA) and Risk Management functions to establish a robust international management strategy.
- Medical Directors Forum (MDF) : Lead and drive the EU Medical Directors Forum, sharing insights and innovations and improving outcomes. Engage with peers and experts to optimize patient care, outcomes, and benefit management.
- Local Medical Affairs Strategic Plan : Lead European countries in developing and executing Local Medical Affairs plans, aligned with local priorities and Global guidance. Help the affiliates where appropriate in delivering symposia at local congresses, internal and external educational meetings, local publications, and Key Opinion Leader (KOL) identification and development.
- KOL Engagement Plans : Support European countries in creating national and regional KOL plans. Develop site-specific advocacy plans, including Advisory Boards and Educational Symposia.
- Collaboration and Silo-Breaking : Foster collaboration across a multi-matrixed organization by breaking down silos.
- Promote change : Embrace change as an opportunity for innovation.
- Regulatory Compliance and Quality : Ensure compliance with European and international regulations, internal Standard Operating Procedures (SOPs), and deliver scientifically sound content of high quality.
- Effective Communication : Facilitate information exchange and align activities among therapeutic areas, CSL Vifor, and partners.
Qualifications
- Medical Doctor (M.D.): this is an absolute requirement
- Minimum 15 years industry experience including Medical Affairs at affiliate as well as at regional and global HQ level.
- Ideally post-graduate specialization in Pharmaceutical Medicine and qualification in marketing and/or business administration (MBA/eMBA)
- Proven relationship building competencies with external stakeholders
- Strong commercial acumen
- Significant and proven track record of excellence in the pharmaceutical industry
- Must have medical affairs experience including launching new products, market shaping and launch readiness activities
- Experience of working in a European/Global medical affairs role and with commercial teams
- Experience managing cross-functional projects and teams
- Excellent understanding of healthcare systems in Europe and the needs of payors
- Must have experience: pre-launch and launch phase, in running Phase IV studies and lifecycle management of mature products
- Experience in establishing scientific relationships/interactions with academic societies
- Leadership experience from previous positions in leading large teams
- Finance and budgeting experience
- Professional level in English, both in oral and in written communications and fluency in other language(s), e.g. German, French and/ or Spanish highly desired
- Excellent user of Office Programs (Word, Excel, PowerPoint)
- This role will demand an ability to work strategically and operationally in equal measures. The successful candidate will be a self-starter, who thrives in ambiguity and possesses an entrepreneurial and innovative approach.
CSL Vifor aims to become the global leader in iron deficiency and nephrology.
The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.
For more information, please visit viforpharma.com
We want CSL to reflect the world around usAs a global organization with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.
Do work that matters at CSL Vifor #J-18808-Ljbffr