Description
Senior Regulatory Affairs Specialist/Manager positions - Global Clinical Research Organisation - flexible home working - Up to £60,000Senior Regulatory Affairs Specialist/Manager positions - Global Clinical Research Organisation - flexible home working - Up to £60,000
We are currently working with a leading global CRO who provide full-service drug development services to many of the top 10 pharmaceutical companies.
Due to recent developments, they have taken on a number of high profile projects and are looking for experienced Senior Regulatory Affairs Specialists to work on behalf of one of the leading pharmaceutical companies. This role will have the flexibility of working from home and paying up to £60,000.
Key Skills/Experience
- Candidate must have previous experience working on clinical trials within the Pharmaceutical/CRO industry
- Bachelors degree in Chemistry or Life Sciences, Nursing or equivalent experience
- Coordinate and manage regulatory & ethics committee submission and maintain approvals throughout EMEA, Asia Pacific and Latin America regions
- Preparation of technical documentation, such as IMPD's and IB's
- Ability to comply with SOP's, ICH GCP and national regulations as applicable
- Good knowledge of ICH GCP and the EU Clinical Trials Directive/National regulations
The company offers the opportunity to work across a number of new and exciting projects and exposes you to work closely alongside some of the worlds top leading pharmaceutical companies.
If this is of interest to you and you would like to find out more information on this position or any other regulatory affairs positions, please contact Amanda Edwards on or please email a.edwards(a)realstaffing.com Sthree UK is acting as an Employment Agency in relation to this vacancy.