Regulatory Affairs Lead - Drug Development

South West England  ‐ Onsite
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Regulatory Affairs Lead - New Drug Development - SME Pharma - Up to £65,000

Regulatory Affairs Lead - New Drug Development - SME Pharma - Up to £65,000

Do you have stronmg regulatory affairs experience working for a large or small pharmaceutical company? Have you got experience working on products in development and leading them through to MAA submission? Do you like to manage your own time, have responsibility for your own portfolio and be able to influence the direction of a company? This role might be for you! This company is looking for someone with the below, please apply if you think you fit the bill:

You will need to have:

- Strong pre approval regulatory affairs experience

- European regulatory affairs experience

- Phase II and III and CTA experience

- Previous experience compiling and submitting an MAA

- Strong project management/management 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:
717658
Contract type
Permanent
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