Clinigen is seeking a Strategic Regulatory Medical Writer to support the company's continued growth. The role involves preparing high-quality regulatory documents and providing strategic writing support across the drug development lifecycle.
Requirements
- Lead the preparation and oversight of high-quality regulatory documents and slide decks
- Maintain Global Marketing Authorisations for allocated projects
- Provide strategic regulatory writing support across the drug development lifecycle
- Work on project-based assignments with a diverse client base
- Collaborate within small expert-led teams
- Own documents through all drafting stages
- Interpret complex scientific and regulatory data
- Support clients in preparing for regulatory agency interactions
- Contribute to regulatory intelligence activities
Benefits
- 27 days holiday plus bank holidays
- Discretionary Bonus Scheme
- Pension contributions 5% matched
- Life assurance 4 x annual salary
- Flexible Benefits Platform with £25/month Company contribution
- Annual salary review
- Independent financial advice service
- Enhanced Employee Assistance Programme
- Shopping discounts with retailers
- Long service awards
- Recognition scheme & employee of the year awards