Regulatory Affairs Project Manager - Pre approval

South West England  ‐ Onsite
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Description

Regulatory Affairs Manager - Full Life cycle management - Drug development experience - Up to £60,000

Regulatory Affairs Manager - Full Life cycle management - Drug development experience - Up to £60,000

We are currently working with a leading global regulatory affairs company currently looking to expand their regulatory affairs team. They are looking for an experienced professional that can take responsibility for the product portfolio, be involved in developing their products and leading from the front. They have 1 product at the pre submission stage that they are looking to take through development and lead to MAA submission.

You will need to have:

- Strong pre approval regulatory affairs experience

- European regulatory affairs experience

- Phase II and III and CTA experience

- Previous experience MAA experience

- Experience of leading your own projects (no line management experience needed)

- DCP experience a must

The company are an excellent company to work for. They have a great company culture, value their employees and really encourage career development. The company are continuously growing however they continue to maintain the 'family feel' projected across all departments. This is an opportunity for you to shine and prove yourself with your excellent regulatory skills.

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
Start date
05/2014
From
Real Staffing
Published at
03.06.2014
Project ID:
717654
Contract type
Permanent
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