Global Medical Affairs Director Cardio Renal Metabolic
Inseriert am: 22.04.2020
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Job ID287763BRPosition TitleGlobal Medical Affairs Director Cardio Renal MetabolicApply to Job
Job Description
50 Million! That is the number of how many patients with atherosclerotic cardiovascular disease worldwide do not achieve LDL-C lowering goals and remain at increased risk despite being on current standard of care.
As part of Novartis, you are committed to reimagine medicine and be part of a remarkable team that shares the vision to transform clinical practice for patients with cardiovascular disease. You will also realize your potential while interacting with a outstanding employee community, working side by side with talented individuals and collaborating with the most respected academic institutions. Some of the best leaders in the industry will inspire you. This is a role waiting for you to put your own stamp on it.
As our Global Medical Affairs (GMA) Director, you will be responsible for providing medical and scientific leadership into medical brand teams and other brand related functions from pre-launch through the whole life cycle of the compound. You will support the Global Brand Medical Director (GBMD) in the execution of GMA activities in alignment with GMA& Health Economics and Outcomes Research (HEOR) functions.
Your responsibilities will include:
• For the assigned Medical Affairs studies (Phase IIIB-IV, PMS, observational studies without regulatory impact) within program/brand, provide medical scientific input and delivery when appropriate.
• Serve as a disease area scientific and medical expert for internal customers/stakeholders, e.g., GCT, Scientific Review Committee, research, exploratory development, device development, Marketing, Novartis local medical organizations, and other line functions within GMA and external customers e.g., Key Opinion Leaders (KOLs) and patient advocacy groups
• Build together with the GBMD/Portfolio GBMD a highly influential medical and scientifically based platform.
• Provide medical scientific input for the assigned program/brand(s) to co-develop with the appropriate functions an integrated Product Strategy (IPS), MA strategy and related MA plan as well as develop the medical affairs section of the clinical development plan.
• Provide guidance to CPOs related to their MA study program; review, approve and follow up on local MA studies
• Execute with the GMA team the global scientific communication plan
Minimum requirements
What you’ll bring to the role:
• PhD with unique knowledge for successful clinical program development and execution, with ≥ 3 years of clinical research experience required OR
• MD with specialty with board certification or equivalent, with ≥ 3 years of clinical research experience required
• Medical Affairs and/or Market access experience
• Medical and/or scientific expertise within disease area required and/or experience in having launched a vaccine
• Experience in having launched a medication in a regional/global market
• Demonstrated ability to establish strong scientific partnership with key investigators in assigned TA, academic institutions and scientific societies
• Fluent English (Oral and Written)
• Advanced medical/scientific writing and communication skills.
• Strong track record of collaboration in a matrix environment
WHY CONSIDER NOVARTIS?
750 million. That’s how many lives our products touch. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives?
We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks.
We are Novartis. Join us and help us reimagine medicine.DivisionPHARMABusiness UnitGLOBAL MEDICAL AFFAIRSLocationSwitzerlandSiteBaselCompany/Legal EntityNovartis Pharma AGFunctional AreaResearch & DevelopmentJob TypeFull TimeEmployment TypeRegularShift WorkNo
