Jobs & News

A Senior Regulatory Consultant position is available that can be carried out from home or in the French Office.

This position requires someone with at least 4 years regulatory experience in EU product maintenance as the role relates to life-cycle management. Project management experience is required as the ideal candidate will be responsible for developing regulatory strategies for the life cycle management of approved products.

Ideally the preferred candidate should have direct EU experience (MRP, DCP and Centralised) and experience in the technical aspects of pharmaceutical product manufacture. Familiarity and experience with eCTD is essential, as is good communication skills.

The roles JOB03002, JOB03003 & JOB030004 will pay up to 100,000 GBP.

If you are interested in this position please send a copy of your CV to jobs@ipcons.co.uk with the reference JOB03002 in the subject line. Closing date for submissions 14 March 2011.

A full-time permanent position is available in South London for a Regulatory Manager responsible for new products.

This position requires someone with at least 3 years regulatory experience and with at least 2 years of EU experience. This should also include 1 years man-management experience.

Ideally the preferred candidate should have direct EU experience (MRP, DCP and Centralised) and experience in the technical aspects of pharmaceutical product manufacture.

The role will pay in the region of 50,000 GBP plus benefits.

If you are interested in this position please send a copy of your CV to jobs@ipcons.co.uk with the reference JOB03001 in the subject line. Closing date for submissions 14 March 2011.

Independent Pharma Consultants are now promoting various job opportunities for full-time, part-time and consultancy roles. Please bookmark the News and Jobs section and return often to check for new positions.

If you are interested in any of the roles please quote the reference number and send a copy of your CV (in .doc or .pdf format) to jobs@ipcons.co.uk and we will try our best to place all suitable candidates.

- Happy Job Hunting from all here at IPC -

Out of the many varied regulatory affairs services Independent Pharma Consultants offers to the pharmaceutical and healthcare industry, we are intending to grow our training courses in 2011.

We already offer an extremely effective and popular regulatory affairs course called Pharmaceutical Regulatory Affairs in the EU and US that is run through the company Informa, and have provided various in-house courses to the industry.

We now intend to add to our portfolio and provide courses in various areas of regulatory affairs, including:

1. Pharmacovigilance
2. Preparing effective eCTD submissions
3. PIPs
4. Handling and responding to regulatory authorities

If you are interested in learning more please do not hesitate to contact us.

It is now 5 years since it became mandatory for companies to conduct user (readability) testing on Patient Information Leaflets that accompany medicines. We here at IPC (and PIL2005.com) are very keen to discover just how successful this programme of user testing has been.

We are currently looking at ways to test the effectiveness of the methods used over the last 5 years and to determine from patients how successful the "improvements" have been.