Msl Kidney Care (Fixed-Term Contract)
Vantive: A New Company Built On Our Legacy Baxter is on a journey to separate our ~$5B Kidney Care segment into a standalone company. Vantive will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us.
At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us are driven to help improve patients' lives worldwide. Join us as we revolutionize kidney care and other vital organ support.
Summary The Medical Scientific Liaison (MSL) will provide clinical and technical expertise to the Therapeutic Areas (TAs) "Kidney Care" and will have clinical knowledge for the entirety of the product line(s) related to these TAs. Together with the Regional Medical Manager, the MSL will be accountable for the implementation of the medical strategy down-stream from Global TA.
The MSL is responsible for aligning the Voice of Customer (VOC) with the respective Global Therapeutic Area Leaders and clinical development teams.
What you'll be doing Contribute to the development and implementation of cluster business strategies and tactics to optimize markets for current and future products and development of rational strategic and tactical plans (like launch plans, BaxP). Provide clinical expertise for the creation, development and delivery of high value-added medical-to-medical educational programs that support commercial team's efforts and deliver medical-to-medical evidence-based presentations and discussions to external medical teams and HCPs to support therapy adoption. Identify and engage with KOLs and "rising stars" of the respective area of responsibility, establish and maintain peer-to-peer relationships to build awareness, proper use and investigate new uses of products. Liaison with medical organizations and external subject matter experts (KOL'S) within the scope of the Therapeutic Area, e. g. , as clinical investigators or scientific consultants. Responsible for creation and facilitation of scientific Advisory Boards. Provide scientific support and attendance at conferences and meetings in the respective areas of responsibility. Review/approve cluster related advertising and promotional, as well as scientific and educational, materials within the therapeutic areas of responsibility and ensure all cluster advertising and promotional, as well as scientific and educational materials comply with country requirements. Provide input into clinical research strategy and facilitate Phase IV clinical research like registries for launch and licensed products and give input on new product development for successful launch into the marketplace. Maintain knowledge base as to developments and trends in medical sciences. Compliance to Ethics, Compliance, internal and external policies. What you'll bring Clinical healthcare professional background, preferably with renal or acute/ICU experience, and/or industry experience in Medical Affairs are preferred. Effective interpersonal, analytical and problem-solving skills. Effective critical thinking skills and strategy development. Ability to work independently and in groups in a collegial manner to manage projects and timelines. Excellent skills for building and maintaining very good relationships with external experts. Excellent medical writing and oral communication skill. Fluent Knowledge of English language, written and spoken. Willingness to travel across the cluster.
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