Home
CANDIDATES
Login / Register
Latest Science Jobs
Preview All Jobs
Our Service
Testimonials
Personality Testing
Non EU Candidates
EMPLOYERS
Login / Register
Our Service
Why Seltek
Testimonials
Register Vacancy
Getting Work Permits
TOOLBOX
Tips for Success
TOOLS OF THE TRADE
Weblog
Sales Training
Recommended Reading
Contact Us
Links Directory
Site Map
Complaints Policy
HotSheet Newsletter
Work Permits & Visas
Medical Jobs
Medical jobs are our business. Below you'll find a selection of the type of jobs we handle. These are not current vacancies, you'll need to click here to find a list of our latest jobs.
|
Job Title
|
CRA II | ||||
|
Job Details
|
This is an exceptional opportunity to join one of the fastest growing CROs with full service capability on an international level! Due to recent growth and business development activities an opening for a CRA II has become available within the clinical operations group based in the South East. This rôle will have European scope and offers the chance to develop further your exisiting site management skills. As a CRA II you will be responsible for all aspects of site management for a number of studies across phases II-IV of development and a broad range of therapy areas. Travel is essential in this rôle and you can expect to be monitoring within the UK and Europe for 40% of the time. As you gain more experience you will become involved in document review, staff training and the mentoring of junior CRAs. There is a competitive remuneration package available to the right candidate including pension, healthcare, life assurance, 23 days holiday and company car allowance. Call now for a confidential discussion about this exciting rôle! | ||||
|
Basic
|
£24000 |
OTE
|
£24000
|
Job Title
|
SENIOR REGULATORY AFFAIRS ASSOCIATE |
|
Job Details
|
An exciting opportunity within European regulatory affairs! Our client a global CRO with blue chip pharmaceutical/biotechnology companies as clients, is looking for an experienced regulatory affairs associate to complement their existing regulatory team in the UK. In this rôle you will manage assigned regulatory projects, ensuring that they are adequately resourced, quality is maintained, costs are in line with budget, and submission to regulatory authorities takes place within the planned timeframe. You will work mainly on marketing authorisation applications but will also have involvement with NDA and CTD applications. Extensive liaison with regulatory authorities within the UK and Europe and clients will be required in this rôle to ensure the best possible outcome for applications. There is a competitive remuneration package available for the right candidate including pension, healthcare, life assurance, 25 days holiday and relocation assistance. Interested? Call us in the strictest of confidence to find out more! | ||||
|
Basic
|
£50000 |
OTE
|
£50000
|
||