Provide support, where required, in the preparation for Regulatory Agency meetings (eg scientific advice).
Support the preparation of other regulatory documentation.
Provide input to regulatory strategies for development products
Maintain current knowledge of relevant legislation in the UK, EU, US and all appropriate guidelines (including ICH).
A degree or equivalent in a Life Science subject.
3-5 years of regulatory experience with a significant proportion managing Phase I-III clinical trials, ideally within a CRO or a small biotech company.
Demonstrated ability to work with cross functional teams.
Strong medical or technical writing skills and attention to detail.
Please use a cover letter to highlight how you meet the criteria for the role (highlighting your experience) Your cover letter along with your CV will be used to assess your application.
Real Staffing, a trading division of SThree Partnership LLP is acting as an Employment Agency in relation to this vacancy| Registered office | London, United Kingdom | Partnership Number | OC387148 England and Wales