Executive Director, Oncology Cell & Gene Therapies
Executive Director, Oncology Cell & Gene Therapies
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$ 248500 - 461500
1 Vacancy
Job Description
Band
Level 7Job Description Summary
Join Our Vision: At Novartis we are on a transformative journey in cell and gene therapy pushing the boundaries of medical innovation building on our heritage pioneering this field.We are currently seeking an experienced and visionary Executive Director to provide strategic leadership to Cell and Gene (C&G) Therapy within our Global Oncology Medical Affairs department.
In this critical role you will lead the C&G Global Medical Directors and act as the C&G enterprise medical voice for the assets and or disease areas across the lifecycle (early to in-market) and strategic partner to Research Development US and International Medical Affairs for all assets on this platform.
Youll ensure that medical & scientific leadership input is reflected to shape the early portfolio (pre TDP) and that medical practice and patient needs are reflected in the clinical development plans leading to optimal regulatory approval & patient access and support the clinical adoption worldwide.
The Executive Director is also responsible for the implementation of medical strategies for early programs globally with a focus on innovative evidence solutions including interventional studies NIS and RWE studies and implementation science projects.
This role will require you to develop / own the Integrated Evidence Plans (IEP) and provide input into development while ensuring US and Intl medical perspective is reflected.
The Executive Director will also act as a subject matter expert in the development of the overarching strategies providing inputs during design and along the end-to-end execution of programs across different disease areas. You will provide leadership and deep medical expertise in the TA pivoting support based on business priorities and will represent GMA with senior stakeholders when needed.
Job Description
#LI-Hybrid
East Hanover NJ
Key Responsibilities:
Lead development and execute medical affairs strategy for priority programs including transformative tactics such as: research/population health innovative partnerships and integrated evidence plans and proactively provide input to Development on potential new therapeutic indications to enrich Registration Programs and to consider new therapeutic opportunities.
Co-develop plans for evidence generation medical launch plans MSL / Field Medical Affairs strategy medical education programs scientific publication planning and Medical Expert network development with TAs
Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders.
Financial tracking to ensure timely and cost-effective development & execution of medical activities.
Partner with Development S&G US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs.
Represent GMA around prioritized portfolio with internal and external audiences in collaboration with TAs including the investment medical and regulatory communities as well as pharmaceutical or biotechnology industry collaborators/partners.
Represent the voice of the patient internally and evaluate factors relevant to a patients informed decision making.
Ensure GMA activities (incl. Patient Access programs) are designed and executed in compliance with company policy guidelines and highest medical quality standards.
Requirements:
Must have:
MD (Preferred) or PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which is responsible is an advantage.
Demonstrable experience in Pharmaceutical Industry within Medical Affairs and/or Clinical Development. Firm working knowledge of GCP scientific and clinical methodology protocol designs management and regulatory requirements for clinical studies designated for review by regulatory authorities.
Critical thinker and with ability to navigate uncertainty without major supervision. Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change.
People management experience and skills; ability to truly collaborate across functions and markets: serve-partner-co-create. Able to navigate in an environment of shared outcomes and cross-business accountabilities.
Deep understanding of health care systems and key external stakeholders and a strong track record of delivery focus for time and quality in medical affairs projects. Successful development and implementation of innovative programs and processes.
Understands unmet medical needs generates the right evidence to fulfil them uses innovative multichannel communication formats for effective evidence dissemination.
Credibility as peer expert with external stakeholders and an agile mindset & ability to lead in an agile organization across Disease Areas.
Preferred
Highly preferred: Significant medical affairs early asset lifecycle pre-launch and launch experience in Global organizations
Experience in developing and executing Best in Class processes at scale
Clinical trial research experience conducted in a pharmaceutical or equivalent academic environment in Oncology is strongly desired
The salary for this position is expected to range between $248000 and $461000 per year.
The final salary offered is determined based on factors like but not limited to relevant skills and experience and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.
Your compensation will include a performance-based cash incentive and depending on the level of the role eligibility to be considered for annual equity awards.
US-based eligible employees will receive a comprehensive benefits package that includes health life and disability benefits a 401(k) with company contribution and match and a variety of other benefits. In addition employees are eligible for a generous time off package including vacation personal days holidays and other leaves.
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: Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion gender national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.
Accessibility and reasonable accommodations
The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position please send an e-mail to call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Range
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-BeingRequired Experience:
Director
Employment Type
Full-Time
Key Skills
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