BioTalent is collaborating with Big Pharma client based in to appoint a permanent (Senior) Safety Scientist / Associate Director. This role will suit someone with a strong and successful track record in post marketing safety evaluation, new drug applications, regulatory filings, benefit & risk assessment and safety risk management

You will be Responsible For Activities including:
Aggregate case reporting (ICSR), aggregate report (DSUR, PSUR), signal detection/management, safety strategy, input to clinical development strategy (from safety perspective), Risk management (CCDS, IB, RMP, IND/NDA, MAA), support, presentations, publications, vendor relations  

You will bring the following:

Medical Doctor qualification with post qualification clinical/patient facing experience. (Board certification would be a bonus)
+4 years drug development and minimum 2 years drug safety experience in CRO/BioTech/Pharma. 
GxP / Regulated process 

If this role is for you please be in touch to dominic.pritchard@biotalent.com or +44 203 828 6059