Job Description Summary
LOCATION: London UK or Dublin Rep of Ireland
ROLE TYPE: Hybrid Working LI-Hybrid
As a Director Integrated Evidence Planning youll be at the forefront of shaping how Novartis leverages evidence to bring medicines to patients.
This role offers a unique opportunity to lead strategic and operational efforts in developing integrated evidence plans that influence regulatory success market access and clinical adoption.
Youll collaborate across global teams from Medical Affairs to Market Access to ensure our evidence generation is robust innovative and aligned with business goals.
If youre passionate about transforming healthcare through data-driven insights and thrive in a dynamic cross-functional environment this is your chance to make a meaningful impact.
Job Description
Key Responsibilities
- Advise on the development of strategic co-created Integrated Evidence Plans to support regulatory success market success and clinical adoption.
- Guide squads in identifying evidence gaps and prioritizing high-impact opportunities across functions
- Promote patient-centered above-brand evidence strategies to reduce silos and drive innovation
- Apply impact frameworks to assess business value and inform decision-making
- Ensure global relevance by integrating input from priority countries like US China Germany and Japan
- Facilitate external validation of evidence gaps and proposed solutions
- Drive continuous improvement of IEP processes through stakeholder feedback and optimization
- Act as internal thought leader and change agent for Integrated Evidence Planning excellence
- Collaborate cross-functionally to ideate evidence solutions that support labeling access and adoption
- Champion a collaborative entrepreneurial culture that embraces innovation and true integrated evidence generation.
Essential Requirements
- Advanced degree in life sciences or healthcare; MBA or equivalent preferred
- Solid experience in pharma academic research or healthcare with focus on evidence generation
- Proven leadership in cross-functional teams and managing change in complex global environments
- Strong expertise in interventional non-interventional trial design and real-world evidence methodologies
- Excellent communication skills to translate complex concepts for diverse global audiences
- Quickly build credibility influence and respect; set ambitious goals; and inspire collaboration among peers and stakeholders
Desirable Requirements
- Deep understanding of drug development regulatory landscapes and healthcare systems across geographies
- Extensive industry experiences generating evidence for assets across different stages of drug development.
Why Novartis:
Our purpose is to reimagine medicine to improve and extend peoples lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:
receive:
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.
Commitment to Diversity and Inclusion:
Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.
Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities join the Novartis Network here: Desired
Agility Agility Clinical Practices Cross-Functional Collaboration Data Analysis Drug Development Employee Development Healthcare Sector Understanding Health Sciences Influencing Skills Innovation Inspirational Leadership Integrated Evidence Generation Medical Affairs Medical Communication Medical Education Patient Care People Management Pharmaceutics Priority Disease Areas Expertise Product Launches Product Strategy Real World Evidence (RWE) Regulatory Compliance Research Methodologies 4 more