Medical Lead
hace 4 semanas
Job ID- 366116BR- Mar 09, 2023- Spain**Job Description**:
- 365 days a year, our global network operates works to ensure our patients have the treatments they need to live longer, healthier lives.
- The purpose of this role is to focus on optimizing patient access and outcomes by providing up-to-date compound and disease area medical expertise, 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 key responsibilities**:
Your responsibilities include, but are not limited to:
- 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.
- Lead early identification of strategic drivers, elaboration of patient journey, positioning, target population, the wider stakeholder population mapping and segmentation.
- 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 Omnichannel where possible.
- Gathers and internally shares relevant captured insights (advisory boards, events etc),
- 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.
- Identifies Real World Evidence (RWE) needs and utilizes implementation science and other innovative methodologies
- 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.
- Provides key medical expertise on the company's pipeline programs, disease 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.
- Raises awareness of Novartis' brands, programs, and disease areas through publication of manuscripts, scientific presentations, projects and educational trainings as well as acts as company ambassador in external scientific programs and congresses.
**Diversity & Inclusion / EEO**:
- Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve._
**Minimum Requirements**:
**What you’ll bring to the role**:
**Essential**:
- Education background
- MD, PhD or BSc with strong experience in Health Sciences.
- English and Local language: fluent spoken & written
- **Seniority in Medical Affairs (Medical Lead and/or MSL, greater than 4 years’ experience in Medical Affairs)**:
- Pharmaceutical industry experience
- Significant clinical and research background GCP
- Strong medical and scientific bases and agility to transverse the diseases' arena
- Good planning and organizational skills as well as strong communication skills and customer orientation
- Strong medical and scientific writing skills
- Preferred experience in innovative study designs e.g. RCT/RWE mixed designs as well as preferred proven track record of co-creation and co-execution of protocols with stakeholders in healthcare systems
**You’ll receive**:
Company Pension Plan; Life and Accidental Insurance; Meals, Allowance or Canteen in the office; Flexible working hours.**Why consider Novartis?**
769 million. That’s how many lives our products touched in 2020. 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 brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and
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