Search results
Search Results with no keywords
Salary: Up to £70,000
Date Posted: Thursday, 11th of March 2010
Description
We are recruiting for a Medical Advisor to join an established Pharmaceutical company in Hertfordshire. You will be the Medical Affairs support for brand tactics such as campaign and materials updates, reporting to the European Senior Medical Advisor. As Medical Advisor you will be providing in-depth knowledge and training to…more info »
Click here to view this job
Salary: £20 - £28
Date Posted: Wednesday, 10th of March 2010
Description
We are recruiting for a Medical Writer I/II to join an established Pharmaceutical company based in Berkshire. You will ensure that all clinical documentation for R&D project are sourced, tracked, reviewed, completed and processed in a quality, timely and accurate manner for regulatory submission.
Key responsibilities
- Prepare clinical…more info »
Click here to view this job
Salary: Competitive
Date Posted: Wednesday, 10th of March 2010
Description
We are recruiting for a Senior Medical Writer to join an established Pharmaceutical company based in Berkshire. You can be home based depending on the level of your experience. You will ensure that medical writing documents are preparedaccording to appropriately rigorous, objective and informative medical writing procedures and processes.…more info »
Click here to view this job
Salary: 0
Date Posted: Wednesday, 10th of March 2010
Description
Regulatory Affairs Manager - Emerging Markets
You will be responsible for:
- Using your knowledge of internal regulatory affairs to provide input into product strategy for the IE region.
- Preparing internal market applications for new products.
- Reviewing post market variations.
Key activities: …more info »
Click here to view this job
Salary: UP to £16 phr
Date Posted: Wednesday, 10th of March 2010
Description
We are recruiting for a Junior Medical Writer / Publisher to join an established Pharmaceutical company based in Berkshire. You will provide ongoing support to the Publishing group. You will be required to ensure that all clinical documentation for assigned projects are located and sourced from the internal archive.…more info »
Click here to view this job
Salary: 0
Date Posted: Wednesday, 10th of March 2010
Description
Regulatory Affairs Manager - Emerging Markets
You will be responsible for:
- Using your knowledge of internal regulatory affairs to provide input into product strategy for the IE region.
- Preparing internal market applications for new products.
- Reviewing post market variations.
Key activities: …more info »
Click here to view this job
Salary: 0
Date Posted: Wednesday, 10th of March 2010
Description
Regulatory Affairs Senior Manager - Nephrology and Inflammation
Key activities
- Participate through the Global Regulatory Team in the development of product label and core data sheet.
- Respond to requests from the Global development team and functional areas.
- Advocate and actively support regulatory compliance.
-…more info »
Click here to view this job
Salary: 30000 - 40000
Date Posted: Tuesday, 9th of March 2010
Description
Quality and Regulatory Compliance (QRC) Advisor
Our client are a leading company in their field producing integrated data management software for clinical trials and drug safety. Their products are designed to enable life science companies to automate and integrate the management of their entire clinical development process.…more info »
Click here to view this job
Salary: £45,000
Date Posted: Tuesday, 9th of March 2010
Description
We are recruiting for a Quality, Regulatory and Pharmacovigilance Compliance Manager with a leading provider of integrated data management software for clinical trails and drug safety based in Berkshire. In this specific role you will provide compliance support to the company's software development and service delivery operations relating to an…more info »
Click here to view this job
Salary: 35000 - 45000
Date Posted: Monday, 8th of March 2010
Description
Senior Regulatory Affairs Executive
Reports to: Regulatory Affairs Manager
Job accountabilities:
- Maintenance of clinical trial and marketing authorisation applications.
- Preparing and submitting applications to the relevant authorities.
- Keep up to date with legislation's affecting pharmaceuticals in UK and Europe.
- Preparation and maintenance…
more info »
Click here to view this job
