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Level 4Job Description Summary
#LI-Hybrid (3 days per week on-site)Job Description
Major Responsibilities:
Implement regional regulatory strategies in alignment with global objectives.
Contribute to global regulatory planning and identify strategic gaps or risks.
Lead or support Health Authority (HA) interactions including briefing material preparation.
Coordinate timely and compliant regulatory submissions across assigned regions.
Review and approve Clinical Trial Applications (CTAs) Investigational New Drugs (INDs) and Risk Management Plans.
Act as a liaison with local HAs (e.g. FDA EMA) as required.
Ensure timely and effective responses to HA queries and requests.
Collaborate cross-functionally to align regulatory plans with business goals.
Monitor and ensure compliance with internal policies and external regulations.
Support or lead negotiations for regional approvals to meet project timelines.
Essential Requirements:
Bachelors or Masters degree in Life Sciences Pharmacy or a related field.
Proven experience in regulatory affairs within the pharmaceutical industry.
Strong understanding of drug development and clinical trial processes.
Experience in managing regulatory submissions and HA interactions.
Commitment to Diversity and Inclusion/EEO
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 our Novartis Network:
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Read our handbook to learn about all the ways well help you thrive personally and professionally: Desired
Clinical Trials Detail-Oriented Drug Development Lifesciences Negotiation Skills Regulatory ComplianceRequired Experience:
Exec
Full-Time