Precision Medicine Director
Novartis
Barberà del Vallès, Catalunya, España
Full-Time
Competitive
HybridDirector
Job Description Summary
#LI-HybridJob Description
Job Description
About the Role
The Precision Medicine Director leads the development and execution of precision medicine strategies in support of clinical programs, ensuring alignment with broader disease area and global development strategies.
This role operates at the intersection of clinical development, biomarker science, and diagnostics, leading cross-functional teams to design and implement biomarker strategies. The position plays a critical role in enabling patient selection, supporting regulatory submissions, and ensuring high-quality, compliant delivery of clinical and diagnostic programs.
Key Responsibilities
Develop and execute precision medicine strategies aligned with disease area and clinical program objectives
Lead cross-functional biomarker sub-teams covering molecular epidemiology, assay development, and data analysis
Serve as a core member of global clinical teams and act as subject matter expert in precision medicine
Contribute to diagnostic target product profiles and companion diagnostic development strategies
Identify and manage risks to ensure successful delivery of precision medicine programs
Author biomarker and diagnostic sections of key clinical development documents
Support regulatory submissions as a precision medicine and biomarker expert
Facilitate collaborations with external academic and scientific partners
Ensure compliance with applicable medical device regulations and internal quality standards
Promote knowledge sharing and contribute to operational excellence and process improvement
Essential Requirements
Significant experience in clinical research, clinical trials, or precision medicine within a life sciences environment
Proven experience leading cross-functional and multi-disciplinary teams
Strong understanding of biomarker strategies, companion diagnostics, and clinical development processes
Experience working within regulated environments and complying with global regulatory standards
Strong leadership, stakeholder management, and collaboration skills
Ability to manage risk and drive strategic decision-making
Experience developing clinical or regulatory documentation
Strong scientific and analytical capabilities within life sciences
Desirable Requirements
Experience supporting global regulatory submissions for diagnostics or biomarker strategies
Experience working with external academic or research collaborations
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.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future
together? https://www.novartis.com/about/strategy/people-and-culture
You’ll receive:
Competitive salary, Short term incentive bonus, Pension scheme, Health insurance, 25 days annual leave, Flexible working arrangements, Employee recognition scheme, learning and development opportunities
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
Skills Desired
Budget Management, Clinical Research, Clinical Trials, Coaching, Cross-Functional Teams, Lifesciences, People Management, Risk Management, Risk Monitoring