Aktuelle Jobs im Zusammenhang mit Director, International Medical Affairs - Oberwil b Zug - Blueprint Medicines Corporation
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Associate Director, International Medical Affairs
vor 5 Monaten
Zug, Schweiz Blueprint Medicines Vollzeit**Associate Director, International Medical Affairs Operations** Location(s): Zug, Switzerland Level of position: Associate Director Position type: office-based Reporting Line: VP Medical Affairs, International ***How will your role help us transform hope into reality?** ***This position reports into the VP of International Medical Affairs and will...
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Senior Director, Regulatory Affairs
vor 4 Wochen
Oberwil b. Zug, Zug, Schweiz Hologic VollzeitJob Title: Senior Director, Regulatory AffairsAt Hologic, we are committed to empowering people to live healthier lives everywhere, every day. As a leading innovator in women's health, we are seeking a highly skilled and experienced Senior Director, Regulatory Affairs to join our team.About the RoleWe are looking for a seasoned regulatory affairs...
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International Government Affairs Director
vor 5 Monaten
Zug, Schweiz Exact Sciences Corporation VollzeitPosition Overview The International Government Affairs Director, Switzerland is responsible for coordinating activities with external stakeholders (political, patient, and others) focused on market access for Exact Sciences products in target expansion markets around the world. Collaborating closely and cross-functionally with the Medical, Market Access,...
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Senior Director, Regulatory Affairs
vor 2 Monaten
Oberwil b. Zug, Schweiz Hologic VollzeitAs a leading innovator of womens' health, we at Hologic are empowering people to live healthier lives everywhere, every day, Our regulatory affairs team is responsible for keeping abreast of new, changing and existing regulatory requirements. They lead the development and implementation of a global vision for regulatory affairs to influence strategic and...
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Zug, Schweiz Blueprint Medicines Vollzeit**Location(s)**:Zug, Switzerland **Level of position**:Associate Director **Position type**:office-based **Reporting Line**:VP Medical Affairs, International **How will your role help us transform hope into reality?** This position reports into the VP of International Medical Affairs and will work very closely with the country medical affairs...
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Senior Director of Regulatory Affairs
Vor 3 Tagen
Zug, Zug, Schweiz Hologic, Inc. VollzeitJob SummaryWe are seeking a highly experienced Senior Director, Regulatory Affairs to lead our international regulatory affairs team. As a key member of our organization, you will be responsible for developing and implementing global registration strategies to ensure compliance with local and regional registration requirements.Key ResponsibilitiesDevelop and...
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Senior Director, Regulatory Affairs
vor 3 Wochen
Zug, Zug, Schweiz Hologic, Inc. VollzeitJob Title: Senior Director, Regulatory AffairsAt Hologic, Inc., we are committed to empowering people to live healthier lives everywhere, every day. As a leading innovator in women's health, we are seeking a highly skilled and experienced Senior Director, Regulatory Affairs to join our team.Job Summary:The Senior Director, Regulatory Affairs will be...
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Senior Director, Regulatory Affairs Lead
vor 2 Wochen
Oberwil b. Zug, Zug, Schweiz Hologic VollzeitJob SummaryAs a leading innovator in women's health, Hologic is empowering people to live healthier lives everywhere, every day. Our regulatory affairs team is responsible for staying up-to-date on new, changing, and existing regulatory requirements. They develop and implement a global vision for regulatory affairs to influence strategic and operational...
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Director of Regulatory Affairs
vor 1 Monat
Oberwil b. Zug, Zug, Schweiz Viatris VollzeitAbout the RoleWe are seeking a highly skilled and experienced Director of Regulatory Affairs to join our team in Switzerland. As a key member of our regulatory affairs team, you will be responsible for leading the Swiss regulatory team and ensuring compliance with local and international regulations.Key ResponsibilitiesLead the Swiss regulatory team to meet...
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Senior Director, Regulatory Affairs
vor 2 Wochen
Zug, Schweiz Hologic VollzeitAs a leading innovator of womens' health, we at Hologic are empowering people to live healthier lives everywhere, every day, Our regulatory affairs team is responsible for keeping abreast of new, changing and existing regulatory requirements. They lead the development and implementation of a global vision for regulatory affairs to influence strategic and...
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Senior Director, Regulatory Affairs
vor 3 Wochen
Zug, Schweiz Hologic, Inc. VollzeitAs a leading innovator of womens' health, we at Hologic are empowering people to live healthier lives everywhere, every day, Our regulatory affairs team is responsible for keeping abreast of new, changing and existing regulatory requirements. They lead the development and implementation of a global vision for regulatory affairs to influence strategic...
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Director of Regulatory Affairs
vor 3 Wochen
Oberwil b. Zug, Zug, Schweiz Viatris VollzeitAbout the RoleWe are seeking a highly skilled and experienced Director of Regulatory Affairs to lead our Swiss Regulatory Team. As a key member of our organization, you will be responsible for delivering against or bettering expectations from regulatory stakeholders and ensuring close alignment with relevant Commercial Teams.Key ResponsibilitiesLead the...
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Senior Director, Regulatory Affairs Lead
Vor 6 Tagen
Zug, Zug, Schweiz Hologic, Inc. VollzeitHologic, Inc. is a leading innovator in women's health, empowering people to live healthier lives everywhere, every day.Our global regulatory affairs team plays a critical role in ensuring compliance with local and regional registration requirements as well as company policies.As our Senior Director, Regulatory Affairs, you will oversee international...
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Regulatory Director for Combination Product
vor 5 Monaten
Zug, Schweiz SHL Medical AG Vollzeit**Job Overview** The position of the Director Regulatory for Combination Product, Medical Devices and Emerging Technologies is based in the HQ of SHL Medical AG in Zug. It holds overall responsibility for Regulatory matters related to combination products, medical devices and emerging technologies. The holder is responsible for establishing applicable...
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Associate Director, Medical Advisor Ophthalmology
vor 5 Monaten
Zug, Schweiz Apellis Pharmaceuticals Vollzeit**Reports to**: VP, International Medical Affairs **Position Summary**: **Key Responsibilities Include**: - Partner with Medical Affairs, Access, Development and Commercial teams on key initiatives including clinical trial execution, Regulatory planning and launch planning - Provide strategic input into congress and publication plans - Provide strategic...
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Medical Operations Manager, Europe
vor 1 Woche
Zug, Schweiz VIVUS LLC Vollzeit: We currently have a position open for a Medical Operations Manager to implement, execute and direct/manage the key medical projects for current and future VIVUS medicines commercialized in Europe. In this hands-on position, you will report to the Director, European Medical Affairs. - Specific responsibilities, in alignment and coordination with the...
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Director of Regulatory Affairs
vor 2 Wochen
Oberwil b. Zug, Zug, Schweiz Viatris VollzeitAbout the RoleWe are seeking a highly skilled and experienced Director of Regulatory Affairs to lead our Swiss Regulatory Team. As a key member of our organization, you will be responsible for delivering against or bettering expectations from regulatory stakeholders and ensuring close alignment with relevant Commercial Teams.Key ResponsibilitiesLead the...
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Medical Operations Manager, Europe
Vor 7 Tagen
Zug, Schweiz VIVUS LLC VollzeitPOSITION DESCRIPTION: We currently have a position open for a Medical Operations Manager to implement, execute and direct/manage the key medical projects for current and future VIVUS medicines commercialized in Europe. In this hands-on position, you will report to the Director, European Medical Affairs. Specific responsibilities, in alignment and...
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Regulatory Affairs Director
vor 4 Wochen
Zug, Zug, Schweiz NonStop Consulting VollzeitRegulatory Affairs Director OpportunityNonStop Consulting is seeking an experienced Regulatory Affairs Director to join our team in Europe. As a key member of our Regulatory Affairs team, you will be responsible for leading European regulatory operations, ensuring compliance, and developing and maintaining procedures.About the RoleLead European Regulatory...
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Senior Director, Regulatory Affairs
vor 1 Woche
Zug, Zug, Schweiz Hologic, Inc. VollzeitEmpowering Women's Health Through Regulatory ExcellenceHologic, Inc. is seeking a highly skilled Senior Director, Regulatory Affairs to join our team. As a leading innovator in women's health, we are committed to delivering innovative solutions that improve lives.The successful candidate will be responsible for leading our international regulatory affairs...
Director, International Medical Affairs
vor 3 Monaten
S/he will report to the VP Head of International Medical Affairs and will play a key role in bringing a transformative therapy to patients in need across multiple geographies. In addition, this position will contribute to the growth and development of the international operations, bringing new perspectives and experience, as well as working closely with the US Medical Affairs team. This role requires collaborative capabilities within a matrixed environment as well as a commitment to “rolling up one’s sleeves”.What will you do?Partner with global medical leads as international medical representative to develop and drive critical medical affairs programs across international markets, aligned to product, corporate strategies.Manage country medical leads and medical science liaison (MSL) team to establish or strengthen professional relationships with the medical and scientific community and compliantly exchange scientific knowledge with global and regional thought leaders, including 1:1 interactions, congress engagements, and advisory boards.Lead and participate in relevant Medical activities, e.g. data generation, medical communication, market access, medical training and education materials.Identify, drive and support strategies and initiatives to help stakeholders identify relevant patients (precision medicine).Support international Pricing & Market Access team by providing medical affairs’ perspectives and input, (including reimbursement dossier reviews, briefing books, etc).Collaborate with partners in distributor markets to coordinate, leverage and adapt medical activities, as well as be the point person for all medical activities.Contribute to building the Medical Affairs as a key strategic function, as well as represent the International Team on global teams.Collaborate cross-functionally with global and local country-base teams, including business partners.Identify and contribute to the development of product lifecycle opportunities, in alignment with disease area strategies.Evaluate potential collaborative research projects with centers of excellence, in collaboration with relevant internal stakeholders.Collaborate internally to clinical trial activities, including ensuring that appropriate institutions and academic centers have opportunities to participate in Blueprint’s clinical programs.Remain at the forefront of the relevant science knowledge, including competitor landscapes.What minimum qualifications do we require? MD, PharmD or PhD with a minimum of 8 years of medical affairs experience within the pharmaceutical industry preferably both at country and above country rolesExperience in people management is requiredAbility to think innovatively and accurately anticipate future consequences and trends.Ability to lead by example and influence others without authority.Have excellent English language ability – both written and verbally.Ability to present to senior management and external opinion leaders with gravitas and influence.Possess strong analytical skills, especially with regard to understanding and interpreting scientific and clinical research and literature and translating the data into value adding information for both internal as external stakeholders.Be a capable self-starter and team player, with strong interpersonal skills.Possess a collaborative mindset. Be adept, nimble, energetic and comfortable in a fast-paced, dynamic and interdependent environment.Capable of taking a hands-on approach and willing to “roll up one’s sleeves” to get the work doneWhat additional qualifications will make you a stronger candidate? Previous Allergy/Immunology, or Hematology/oncology or rare diseases experience is preferredDemonstrated experience in launching products is highly desirable.Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, OptimismWhy Blueprint? At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators – the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.This is the place where the extraordinary becomes reality, and you could be part of it.Patients are waiting. Are you ready to make the leap?Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas: allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a proven track record of success with two approved medicines, including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research, development, and commercial capability and infrastructure, we now aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases including SM and chronic urticaria, breast cancer and other solid tumors.#LI-Remote #LI-NJ1
