Position Details
About this role
This role supports global regulatory strategy and submissions for vaccine and infectious disease products, working closely with international agencies and cross-functional teams.
Key Responsibilities
- Support regulatory agency communications
- Develop global regulatory strategies
- Prepare regulatory submissions
- Conduct research on guidances
- Collaborate with cross-functional teams
Technical Overview
Involves regulatory strategy development, submission preparation, agency communication, and lifecycle management within global regulatory frameworks.
Ideal Candidate
The ideal candidate is a PhD or MD with experience in global regulatory affairs for vaccines or infectious diseases, skilled in regulatory strategy, submissions, and cross-functional collaboration to support product registration and lifecycle management.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience in regulatory affairs for vaccines or infectious diseases, No experience with regulatory submissions or agency communications, Inability to collaborate with global teams
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