Regulatory Program Lead, Immunology

Biopharma Asia; Basel; Hybrid; CHF 120,000 - 180,000; Full time

Job summary

Johnson & Johnson Innovative Medicine is seeking a Senior Analyst, Regulatory Program Management – Immunology. Located in Basel, this role guides regulatory execution for immunology programs, translating strategy into actionable plans and coordinating cross-functional teams to accelerate submissions and launches.

The position emphasizes strong project management, regulatory expertise, and collaboration across Global Regulatory Affairs and clinical teams to ensure robust and timely regulatory

Qualifications

• Minimum of 4 years of industry/business experience with at least 2 years in pharma R&D.
• Project management experience leading cross-functional teams in a matrix setting.
• Strong written and verbal communication skills; ability to translate strategy into action.
• Knowledge of regulatory requirements and global filing processes.

Responsibilities

• Serve as key facilitator within the RPM department to assigned service area.
• Lead operations and onboarding of new processes and system rollouts across RPM.
• Coordinate with GRT on health authority submissions and global filing strategies.
• Translate regulatory strategy into executable, detailed plans for teams.
• Provide operational leadership to update budgets, forecasts, and performance metrics.
• Support GRT meetings and cross-functional collaboration to ensure timely delivery.
• Drive process improvements and embed best practices across programs.

Skills

Project management

Cross-functional collaboration

Regulatory knowledge

Communication skills

Education

Bachelor’s degree

Advanced degree preferred

Tools

Veeva

MS Project

Job description

Johnson & Johnson Innovative Medicine is seeking a Senior Analyst, Regulatory Program Management – Immunology. Located in Basel, this role guides regulatory execution for immunology programs, translating strategy into actionable plans and coordinating cross-functional teams to accelerate submissions and launches.

The position emphasizes strong project management, regulatory expertise, and collaboration across Global Regulatory Affairs and clinical teams to ensure robust and timely regulatory