NEW: EU Regulatory Intelligence & Pharmaceutical Policy Support
Exclusive to The Source - register/apply now
A global pharmaceutical organization is seeking an experienced Regulatory Intelligence consultant to support assessment and implementation planning associated with the EU Pharmaceutical Package.
The consultant will act as an SME on EU pharmaceutical legislation, assessing regulatory, operational and business implications of evolving requirements.
The Role
- Monitor and interpret developments relating to the EU Pharmaceutical Package.
- Conduct regulatory policy, gap and impact assessments.
- Assess risks, opportunities and implementation implications.
- Translate regulatory developments into actionable business recommendations.
- Coordinate cross-functional impact assessments across Regulatory, Quality, Supply Chain, Manufacturing, Market Access, Legal, Medical and Commercial stakeholders.
- Support implementation roadmaps, organisational readiness and gap assessments.
- Develop regulatory intelligence analyses, briefings, leadership materials and decision papers.
- Maintain regulatory intelligence tracking and support alignment between local and global regulatory teams.
Requirements
Minimum 5 years' experience in regulatory intelligence, regulatory affairs or pharmaceutical policy, ideally within a multinational pharmaceutical environment, with strong knowledge of pharmaceutical regulation, policy reform, approval pathways and lifecycle management.
How to Apply
This contract opportunity is exclusive to The Source.
To apply or request further information, please register or sign in by clicking the button below.
