Medical Lead Gene Therapy for Sma

3 settimane fa

Milano, Italia Novartis A tempo pieno

743 million lives are impacted by us, and as a Medical Lead Gene Therapy for SMA you will contribute so that our impact continues extending and being a positive factor in many lives
As Medical Lead Gene Therapy for SMA you will raise awareness of and develop strong advocacy for Novartis Gene Therapies products with key opinion leaders, clinicians and other medically-relevant stakeholders and institutions by cultivating collaborative relationships and engaging in scientific exchange based on rational, evidence-based and scientifically supported medical arguments.

**Your key responsibilities**:

- Identifie,, maintain relationship with, develop and support national and international key Opinion Leaders in the country, in close collaboration with commercial and medical colleagues.
- Developing and leading regional engagement plans with Key Opinion Leaders (KOLs) and other key external stakeholders in Italy that are aligned with the EMEA Medical Affairs plan
- Serve as scientific peer-to-peer resource to disease experts and medical community with up-to-date relevant medical information and product information.
- Contribute into the local Medical affairs brand plan and its subsequent execution of tactics and activities locally
- Input into the selection of local centres for Novartis Gene Therapies sponsored trials. Ensures that Novartis Gene Therapies local clinical trial activities are consistent with the product strategy. Provides input into the protocol synopses, study protocols, and final study reports for local phase IV trials.
- Appropriately responding to unsolicited requests for clinical data in Italy per guidance from GTx leadership.
- Delivering timely, fair balanced, objective, scientific and economic information and education to health care customers and to internal business partners as required by business needs
- Coordinate and tracks national Non-Company-Sponsored Investigator Initiated Trials and ensures the implementation of guidelines included in boundary documents.
- Support KAM in the development of individual key-account’s business plans and in the delivery of the relevant medical initiatives, trainings and programmes.
- Develop contacts with relevant nationally-organized patient groups, ensuring that their legitimate needs are fully considered and where appropriate incorporated into Novartis Gene Therapies medical-marketing strategy / activities.
- Organize national medical advisory boards. Functions as primary contact with local collaborative groups and fosters medical and scientific information exchange with the national medical community. In coordination with KAM, maintains a high profile with regional and local health organisations and in line with Novartis Gene Therapies EMEA strategy.
- Provide regulatory-complaint clinical and scientific training and presentations for internal and external target groups, ensuring fair-balanced and consistent communication of medical and product-medical messages, within the brand and medical strategies. Deals with medical information questions from the field.
- Participate in reviewing, adapting to local requirements and language and approving materials produced by Novartis Gene Therapies EMEA and Country Marketing function, as per current process and SOP.
- Contribute, through medical expertise, to ensuring proper product labelling, reimbursement and funding in the country.
- Consolidate and disseminate medical competitive intelligence to both local and EMEA teams

**Commitment to Diversity & Inclusion**:

- We are 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**:

- 5+ years experience in the pharmaceutical/biotech (preferred) industry required.
- 3+ years experience in medical affairs positions in orphan diseases is strongly preferred.
- Previous experience in successfully-launched biologics or therapeutics is a plus.
- Therapeutic experience in rare diseases, genetics, metabolic disorders, lysosomal storage disorders, gastroenterology or neurodegenerative disorders is strongly preferred.
- Advanced clinical or scientific degree (preferred MD, PharmD, PhD in Biological Sciences) is required.
- Strong project management skills.
- Knowledge of Italian healthcare system and national regulations relating to codes of practice within the pharmaceutical industry.
- Must have excellent communication and presentation skills (both oral and written) and be proficient in MS Word, Powerpoint and Excel.
- Must function well as a member of a cross-functional team.
- Must exert leadership capabilities and thrive in a cross-functional, multi-cultural matrix environment.
- Office is home-based. Travel approximately 60% of working time. Required travel to internal and external medical meetings (congresses - will required some weekends, team meetings).

**Why Novartis?**

743 million lives were touched by Novarti

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