Medical Lead of Neurosciences

hace 5 días

Santiago de Chile Novartis A tiempo completo

766 million lives were touched by Novartis medicines in 2021. We want curious, courageous and collaborative people like you to join our inspiring environment. Here you’re given opportunities to make a genuine impact on our patient driven mission. Here you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Did you ever imagine how many lives could be touched by your daily work?
- The people we serve need you to achieve the extraordinary. That´s why at Novartis we empower you to bring your best self; we value your diversity of thought and trust your ability to make things happen.-
**Job Purpose**:
Focus on optimizing patient access and outcomes by providing up-to-date compound and disease area medical expertise (Neurosciences), acting as a key expert in the relevant therapeutic area assigned, and leading across functions to address external and internal stakeholder needs. To shape and implement the Local and Global Therapeutic Area strategy through innovative integrated evidence generation, engagement on scientific results with internal and external stakeholders, and co-creation with healthcare systems and the scientific community. To co-design clinical development launch and life cycle management of the drug in close collaboration with Country, Regional, and Global team members. To ensure that the best interest of patients and those who care for them are identified and met**Your responsibilities**:
Your responsibilities include, but are not limited to:
- Medical strategic Plans: 1. Prepares and drives the execution of the local Medical Affairs strategic plans aligned and in collaboration with other functions. This plan should be built based on local stakeholder needs and in line with the Franchise and medical strategies as outlined in the Integrated Product Strategy (IPS) Plans. 2. Lead early identification of strategic drivers, elaboration of patient journey, positioning, target population, the wider stakeholder population mapping and segmentation. 3. Identifies opportunities for joint value creation through engagement with the key scientific leaders and other partners in the healthcare systems including Patients and Patient Associations to co-design strategies and studies, advocating in the assigned therapeutic area. Utilizes Ominchannels where possible. 4. Gathers and internally shares relevant captured insights (advisory boards, events etc), to shape the disease area strategy.
- Integrated evidence co-development: 1. Accountable to Co-developing integrated evidence plans and ensuring local execution of these plans beginning at DDP and throughout the lifecycle in partnership with Global Drug Development (GDD), functional partners, healthcare systems, patients and other external stakeholders. 2. Identifies Real World Evidence (RWE) needs and utilizes implementation science and other innovative methodologies, to close the gap ensuring patient and clinical adoption and better outcomes. Responsible for local and global evidence generation submissions. 3. Leads the Post Trial Access (PTA) and Managed Access Programs (MAP) at local level, evaluates Investigator-Initiated research studies and Trials (IITs) and Research Collaborations (RC) for scientific rigor and alignment.
- Medical expertise provisions: 1. Provides key medical expertise on areas and approved brands. Performs comprehensive evaluation of related products passing DDP/FDP to enable effective cross-functional New Product Planning for the Country Pharma Organization (CPO). Provides informed CPO input to Global strategies, protocols, etc if assigned early product portfolio. 2. Raises awareness through publication of manuscripts, scientific presentations, projects and educational trainings as well as acts as company ambassador in external scientific programs and congresses. 3. Provides medical expertise and leadership to functional partners through the life of the product(s). 4. Represents those who practice medicine and brings an understanding of how patients are cared for into the work of their therapeutic area, ensuring that activities are in the best interest of patients and those who manage them. 5. Ensures Target Patient Population Outcomes (TPOs) are updated and relevant, and that they are being tracked, resourced and impacted at CPO level with appropriate regional and global support.

**Commitment to Diversity & Inclusion**:

- Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve._

**Minimum requirements**

**What you’ll bring to the role**:

- MD or PhD/PharmD in Health Sciences (requirement as per country strategy and/or local regulations). Desired: Specialist Degree or specialist qualification related to discipline for which is responsible. Business degree (e.g. MBA).
- English: fluent spoken & written; Local language: preferable (requirement based on country needs).
- Pharmaceut

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