SEC Recruitment

Regulatory Affairs Manager

Location
Europe
Salary
Negotiable
Posted
19 Jul 2019
Closes
16 Aug 2019
Ref
SRASIQ
Contact
Ilyas Nur
Hours
Full Time
Contract Type
Permanent
Experience Level
Management
What you want to know…

You will be responsible for the preparation and reviewing of Regulatory submissions, acting as a project lead on complex projects to support clinical development. The successful candidate will manage Clinical Trial documents whereby information co-ordination is key. The company in question are world renowned and the potential for growth is huge.

About you…

You will possess specific regulatory expertise as well as the following…

*Technical writing experience in regard to IMPDs and IBs will be advantageous
*CTA experience
*Competent in adhering to SOPs
*Be a solid communicator, both verbally and written
*Able to provide input in the improvement of processes
*Strong computer skills

It won't just be your written communication skills put to the test but also your ability to communicate with a range of authors, editors and a variety of stakeholders.

To find out more about this excellent opportunity apply today. If you would like a confidential conversation on how this role will fit with your own needs or experience, then please do get in touch. I can be reached on Ilyas.nur@secrecruitment.com or on +44 207 255 6600.

Regulatory Affairs Manager
Competitive package
Based in Europe - several countries available

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