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Job Location | Slough |
Education | Not Mentioned |
Salary | £35.00 - £55.00 per hour |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Contract, full-time |
Regulatory Affairs Manager | 6 Month Contract | SloughYour New Company A growing global bio pharmaceutical company with a focus on innovation and speciality care is looking for a Regulatory Affairs professional to join their team in Slough. They create and market innovate medicines with a focus on Oncology, Rare Diseases, and Neuroscience. Their focus is to improve patients quality of life by providing them with effective therapeutic solutions to medical needs through their innovative medicines. Your new roleAs the Senior regulatory affairs professional you will be responsible for the planning and execution of regulatory activities for the UK & Ireland. The role will include managing the regulatory submissions for UK&I, which includes preparing, submitting, and following up applications to submit to the MHRA/HPRA. You will also be responsible for regulatory intelligence, which will include keeping up-to-date with regulatory environment, and completing competitor analyses. Finally, you will be responsible for ensuring the regulatory affairs are fully and updating the regulatory systems for planning and tracking of submissions. You will be reporting directly into the Regulatory Affairs Director of UK and Ireland. What you will need to succeedYou will have at least 3 years post approval/post market/ full life-cycle management experience within a pharmaceutical company within the UK&I. You will have previous experience dealing with the MHRA and HPRA. You will have previous successful experience executing submissions within UK&I. You will have a strong attention to detail and the ability to work autonomously. What you will get in ReturnThis is a 6-month contract position at their location in Slough, with 1 month extensions thereafter. What you need to do nowIf you think this role may be suitable for you please click "apply now".