Medical Assessor-£73,000 p.a. + benefits

Job summary

We are currently looking for aMedical Assessorto join our Innovative Medicines within the Healthcare, Quality and Access group.

This is a full-time opportunity, on a permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London. We are currently implementing a flexible, hybrid way of working, with a minimum of 4 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 8 days a month, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly. Remote working is potentially available for some specific roles. Please discuss this with the recruiting manager before accepting an appointment.

Please be aware that this role can only be worked in the UK and not overseas.

TO BE CONSIDERED FOR THIS ROLE, PLEASE COMPLETE YOUR APPLICATION ON MHRA WEBSITE

http://lhrc1a.rfer.us/MHRALIu1FAL

ONLY APPLICATIONS COMPLETED ON MHRA WEBSITE WILL BE CONSIDERED

Main duties of the job

The successful candidate will be reporting to the Head of New Active Substances in Innovative Medicines. You will be required to assess the clinical and regulatory aspects of marketing authorisation applications forchemical or biological products, in a variety of therapeutic fields

About us

The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research.

The objective of the Innovative Medicines team in Healthcare, Quality and Access Group is to drive quality and critically appraise benefits and risks to inform robust decisions on healthcare access including accelerated access pathways. It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable licensing and market access, as well as ensuring compliance with regulations and standards.