Msl Acute Care Centro-sud

**Medical Science Liaison Acute care (**Centro-Sud)** - Acute Care will focus on the management of major bleedings associated with anticoagulant therapy, with the opportunity to work on andexanet alfa, the only antidote for FXa-I. Although these are not frequent events, the clinical outcome is often devastating, with a high rate of permanent inhability or death - This molecule, initially developed by Alexion Pharmaceuticals, is now part of AstraZeneca portfolio, At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible. At AstraZeneca every one of our employees makes a difference to patient lives every day. As **Medical Science Liaison Acute care (Centro-Sud) **you will act as the first point of contact for any medical/scientific aspect or issue related to the assigned products by engaging in Scientific Exchange with AstraZeneca teams, Key External Experts, Health Care Professionals, and Clinical Investigators. At AstraZeneca, Cardiovascular, Renal and Metabolic (CVRM) is one of our main therapy areas because science continues to uncover commonalities between these diseases. With this knowledge, we are daring to do things differently by shifting focus from treating patients with a single disease, to addressing overlapping disease areas and risk factors. This new approach gives us the chance to save vital time and valuable healthcare resources, and most importantly improve patient lives. **MAIN DUTIES AND RESPONSIBILITIES** Reporting to the Acute Care Medical Affairs Manager, you will engage with external specialists to identify medical unmet needs, evidence gaps and gain insight, and delivers presentations in a non-promotional scientific context as determined by global and local Medical Affairs plans. The role broadly includes the following key components: - Support the Field Force in its relationship with medical target groups through a continuous updating on therapeutic aspects related to the relevant pathology and/or products (in cooperation with the Training Department); - Provide medical input to Competitive Intelligence Department, including critical review of competitor data/scientific material; - Develop and maintain contacts with Key External Experts of the assigned territory, and represent the main contact for any scientific/medical aspect; - Identify local medical needs and define a Local Scientific Plan (LSP), according to the Italian and HQ strategies and policies, to be integrated into the local business plan; - Provide input and support to Medical Advisors/Medical Lead and Clinical Operations Team in sites selection and feasibility assessment for national/international trials, and in the management of potential issues related to the implementation and conduct of international/national trials; - Collect and discuss with Investigators the proposal for independent studies (ESR Externally Sponsored Research) in the assigned territory and, according to SOP, fill in the relevant forms for the company’s evaluation and discussion; - Build partnership with Area/Field Manager to implement the LSP through regular contacts and team meetings; - Develop and maintain contacts with Scientific Societies/Communities; - Maintain regular contacts and support the Regional Access Managers (RAM) and the Local Access Managers (LAM) in the assigned territory to ensure alignment of Local Scientific Plans with regional plans through: relationships/scientific projects with regional Health Authorities and management of scientific issues related to the introduction of Company’s drugs into local formularies, respectively; - Other Activities: - Provide support to the Field Force to guarantee high quality scientific standards in the relevant activities (e.g: planning organization and participation at regional scientific events); - Support the Medical Advisers/Medical Lead and Patient Safety Department in the management of AEs (e.g collection of follow-up information); - Manage medical information requests; - Act as country delegate for assigned GMT activities (active participation and support as needed); - Manage all activities and Account relationship according with Company Values, Code of Conduct, Guidelines/Internal procedures and Italian legislation. **ESSENTIAL REQUIREMENTS** - Scientific Degree - Previous Experience as MSL or Medical Affairs > 2 years, or as physician in acute/critical care setting - Fundamental knowledge of basic research, drug discovery, drug development, clinical environment - Knowledge of the local regulatory requirements related to medical affairs activities - Strong leadership capabilities - Excellent interpersonal skills - Project management experience - Communication skills, including communicating complex technical, scientific, or medical information - Ability to work in team - Networking and influencing skills - Understanding of written/spoken English - Willingness to be part of international teams - Domicile in the working ar