Of all our jobseekers who reach final interview stage for a regulatory affairs role, 95% will get an offer. And 98% of these will accept it.
Become a proactive, goal orientated and pragmatic Regulatory project manager within a leading pharmaceutical company.
This is an excellent opportunity to advance your career and gain exposure to CMC Regulatory Affairs in a varied pipeline of products.
Regulatory Affairs Submissions Specialist required to coordinate regulatory submissions within the EMEA region. The successful candidate will be responsible for the planning, review and submission of regulatory documents.
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I work extensively with CRO’s and Consultancies to source “hard to find” industry specialists according to agreed timeframes.
+44(0)20 7002 0239
Plan your next career move with me. My expertise at your service to take your career where you want it to be. Feel free to get in touch.
+44(0)20 7002 0230
I specialise in placing contract Regulatory Affairs professionals in the Life Sciences industry.
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