You manage the development and execution of evidence plans for Remibrutinib, collaborating with various teams to ensure timely access and clinical adoption of the product.
Anforderungen
- •8+ years in Pharmaceutical Industry experience
- •Significant experience in evidence generation activities
- •Expertise in medical affairs tactics and healthcare systems
- •Understanding of unmet medical needs and evidence generation
- •Strong external network and credibility as peer expert
- •Strategic mindset and ability to influence stakeholders
- •Inspiring leader with strong influencing skills
- •Strong collaboration and negotiation skills
- •Strong English language and communication skills
Deine Aufgaben
- •Create, update, and execute Integrated Evidence Plans for Remibrutinib.
- •Ensure timely availability of evidence for access and clinical adoption.
- •Collaborate closely with Biomedical Research and Development teams.
- •Partner with International and US Medical Affairs.
- •Work with Strategy & Growth and Commercial teams.
Original Beschreibung
# Global Medical Affairs Executive Director Remibrutinib
**Basel (City)** | **Full time**
**Job Description Summary**
LOCATION: Basel, Switzerland
ROLE TYPE: Hybrid working, #LI-Hybrid
The Global Medical Affairs Executive Director Remibrutinib acts as enterprise medical voice for Remibrutinib and the associated indications/disease areas across the full lifecycle.
They will lead the Global Medical Affairs asset/ disease area team, chair the cross-functional Program Medical Affairs team PMAT (incl. Scientific Communications (SciComs), Real World Evidence (RWE), International (Int'l) and US Medical Affairs (MA)) and represents it at Global Program Team (GPT).
They will also be responsible for the medical strategy and tactical execution, ensuring the US and Int'l medical perspective is reflected.
**Job Description**
**Major Responsibilities:**
Responsible for the creation, update & execution of the Integrated Evidence Plans (IEP) of Remibrutinib across the indications Remibrutinib is developed in, ensuring the right evidence is available at the right time to enable access and clinical adoption.
Will act as a strategic partner to and close collaborator with Biomedical Research, Development, International Medical Affairs, US Medical Affairs, Strategy & Growth and Intl & US Commercial.
**Skills and capabilities:**
* 8+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development, incl. global experience.
* Significant experience and expertise in evidence generation activities, such as interventional or non-interventional studies and RWE projects.
* Significant experience and expertise in the full range of medical affairs tactics with a deep understanding of health care systems and key external stakeholders such as Healthcare professionals (HCP), payers, medical societies and guideline committees.
* Understands unmet medical needs, generates the right evidence to effectively address them, uses innovative, multichannel communication formats for effective evidence dissemination.
* Strong external network within the indication space, credibility as peer expert with external stakeholders.
* Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change.
* A highly self-aware and inspiring leader who effectively leads large diverse teams (PMATs) in a complex matrix, demonstrating strong influencing skills.
* Equipped with strong collaboration and negotiation skills, the GMA ED constructively resolves conflicts and removes barriers that get in the way of delivering results.
**Languages :**
* Strong English language skills are essential as are strong communication skills to deliver clear, targeted, and scientifically sound presentations to diverse internal, including senior management and external audiences.
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**Commitment to Diversity & Inclusion:** Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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**Skills Desired**
Clinical Practices, Clinical Research, Drug Development, E-Learning, Influencing Skills, Job Description, Leadership, Medical Communication, Microsoft Access, Patient Care, PCB (Printed Circuit Board), Personal Development, Pharmaceutics, Pipeline (Software), Product Placement, Regulatory Compliance, Software Release, Strategic Direction, Well-Being