Medical Affairs Director - Haematology

Novartis Farmacéutica; London; On-site; GBP 80,000 - 120,000; Full time

Job summary

An established industry player is seeking a Medical Director for Haematology to drive innovative medical strategies and evidence generation. This pivotal role involves leading the development of medical affairs strategies, collaborating with diverse stakeholders, and ensuring compliance with the highest medical quality standards. You will play a crucial role in shaping portfolio strategies and enhancing patient access programs. If you are passionate about improving patient outcomes through innovative solutions and have a strong background in medical affairs, this opportunity is perfect for you. Join a mission-driven organization dedicated to reimagining medicine and making a meaningful impact in healthcare.

Qualifications

• 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
• Fluent in English; other relevant languages are an advantage.

Responsibilities

• Lead medical affairs strategy for Haematology priority programs.
• Co-develop evidence generation plans and medical education programs.
• Partner with cross-functions to shape portfolio and enhance clinical practice.

Skills

Strategic mindset

Collaboration skills

Understanding of health care systems

Delivery focus

Communication formats

Regulatory knowledge

Education

MD

PhD/PharmD in Health Sciences

Specialist Degree

Job description

The Global Medical Affairs team acts as enterprise medical voice across the asset lifecycle and leads the medical strategy for the therapeutic area.

The Medical Director role is responsible for the implementation of medical strategies for early programs globally with focus on innovative evidence solutions including interventional studies, non-interventional studies (NIS) and real-world evidence (RWE) studies and implementation science projects.

With extensive experience in drug development, they will be able to lead Integrated Evidence Packages (IEP) in situations with higher scientific complexity and potential regulatory challenges. They 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.

About the Role

As the Medical Director for Haematology, you will provide proactive input to development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities. You will also ensure that Patient Access programs are supported for all brands within Global Medical Affairs (GMA) and that GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards.

MAJOR ACCOUNTABILITIES:

• Lead development and execution of medical affairs strategy for Haematology priority programs including transformative tactics such as: research/population health, innovative partnerships and integrated evidence plans
• Co-develop plans for evidence generation, Medical Science Liaison (MSL) / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with therapeutic areas (TAs)
• Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders
• Prepare Scientific Research Committee (SRC) submissions for TA assets within remit
• Partner with Development, Sales & Growth (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
• Provide direction and input into the development and implementation of successful reimbursement and market-access strategies

REQUIREMENTS:

• MD (Preferred) or PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which you will be responsible is an advantage.
• 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development
• Fluent oral and written English; Other relevant languages are an advantage.
• Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change
• Ability to truly collaborate across functions and markets: serve-partner-co-create
• Deep understanding of health care systems and key external stakeholders
• Strong track record of delivery focus for time and quality in medical affairs projects
• Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination
• Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.

Preferred:

• Experience and expertise in haematology, including launch and pre-launch activities, and clinical trials conduct
• Experience in developing and executing “Best in Class” processes at scale
• Clinical trial research experience conducted in a pharmaceutical or equivalent academic environment in TA of interest is strongly desired

Why Novartis?:

Our purpose is to reimagine medicine to improve and extend people’s 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!

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.