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Minimum 3 years working in a similar role at a Pharma, Biotech or CRO company and a first degree or PhD in Chemistry, Pharmacy or a Biology-based discipline. Preferably the candidate will have worked on Regulatory Applications such as CTAs, Orphan Drug Applications, Scientific Advice, PIPs, MAA Summaries and Overviews, as well as on clinical documentation (e.g. Protocols, CSRs, IBs, etc). The role is likely to involve working simultaneously on different technical, clinical and regulatory documents and Applications, and as such will suit a motivated professional able to multi-task and who enjoys a fast-moving environment.
25/03 - Glasgow - Kinesys Consulting Ltd - Responsibilities.....