At a Glance
- Tasks: Manage regulatory submissions and support projects in a fully remote role.
- Company: Global biotech organisation with a strong product pipeline.
- Benefits: Flexible remote work, opportunity for contract extension, and impactful projects.
- Other info: Great opportunity for career growth in a supportive environment.
- Why this job: Join a dynamic team and shape the future of healthcare across Europe.
- Qualifications: 5+ years in Regulatory Affairs with strong EU knowledge.
The predicted salary is between 60000 - 80000 £ per year.
About the Company
A global biotech organisation with a strong pipeline of development and commercial products across multiple therapeutic areas is looking for a 12-month reg manager to join the team with scope to extend.
Fully remote but you must be based in the UK.
You will be responsible for supporting at least 3 projects, which could be in development or marked products.
Responsibilities
Manage CTA, MAA and post-approval regulatory submissions across Europe.
Support regulatory strategy for development and marketed products.
Provide regulatory guidance to cross-functional project teams.
Support interactions with health authorities, including scientific advice and accelerated pathways.
Contribute to labelling activities and life cycle management.
Monitor regulatory changes and assess business impact.
Conduct regulatory intelligence to support product development and submission planning.
Requirements
5+ years Regulatory Affairs experience within pharma or biotech.
Strong knowledge of EU CTR and MAA procedures.
Understanding of drug development and LCM lifecycle management.
Excellent communication and stakeholder management skills.
Please apply now or reach out to hear more details
