Are you ready to make a significant impact in medical safety?
Novartis is seeking a passionate individual to join our innovative Neuroscience team. You will work with cutting-edge technology, collaborate with experts, and drive excellence in patient safety.
If you're eager to advance your career and be part of a forward-thinking company, we want you on our team!
About the Role
Office Location:
London (The Westworks), United Kingdom
#LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles of our London office)
#LI-Remote Remote (if living beyond 50 miles of our London office)
Alternative Location:
Basel, Switzerland
#LI-Hybrid Hybrid (12 days per month on-site)
Major accountabilities:
Safety Input and Team Participation:
Provide expert safety input to the clinical development program for assigned projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Lead the Safety Management Team (SMT). Responsible for managing safety issues from the formation of the GPT through Life Cycle Management
Safety Strategy Preparation:
Own the projects/products safety strategy and lead the production of medical safety deliverables
Core Global Labelling:
Responsible for initial development and ongoing maintenance of safety information in Core Data Sheet, addressing safety issues in all project/product indications
Signal Detection and Safety Management:
Oversee overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information, based on data from all relevant sources
Regulatory and Professional Inquiries:
Lead the preparation of the safety strategy for health authority responses and collaborate with other project team members. Respond to inquiries from regulatory authorities or healthcare professionals regarding safety issues
Departmental and Functional Goals:
Contribute to and often lead the development of departmental and functional/business unit goals and objectives. Proactively engages in the development of competencies across the Medical Safety Function
Role Requirements:
Medical Degree or equivalent is preferred; PhD, PharmD or equivalent graduate level health care professional degree required
3 years clinical experience postdoctoral
Minimum 5 years' experience in drug development in a major pharmaceutical company (of which 2 years in a global position), including 2 years in safety at an operational or medical position.
Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
Expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information
Experience with (safety or others) issue management
Experience in leading cross-functional, multicultural teams
Languages:
Fluent English (both spoken and written) is mandatory
Additional desirable skills:
Additional languages are an advantage
Neuroscience experience
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
Benefits and Rewards:
Read our handbook to learn about all the ways we'll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Division
Development
Business Unit
Development
Location
United Kingdom
Site
London (The Westworks)
Company / Legal Entity
GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.
Alternative Location 1
Basel (City), Switzerland
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
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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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