Regulatory Affairs Project Manager
Opportunity for an experienced Regulatory Affairs Project Manager with lifecycle management, to join a global blue-chip Pharma Company. Based in the South East.
Global Blue-CHIP Pharma Organisation
Solid product portfolio, both pipeline and marketed
Office based to the West of London
As Regulatory Affairs Project Manager, you’ll support the regulatory vision and leadership of the Senior Regulatory Affairs Manager. You’ll execute these responsibilities by utilizing experience, knowledge of regulatory landscape, passion and creativity to provide patient-centric and compliant regulatory expertise in line with Our Client’s vision. You’ll support the best interests of patients, the Affiliate and interactions with the regulatory agency and other regulatory authorities.
As Regulatory Affairs Project Manager, you’ll represent the Regulatory department and UK affiliate to the wider organization throughout the product lifecycle, contributing to the department's overall success by executing strategies and tactics and meeting objectives in line with business goals and culture. You’ll be an active participant in the business life of the affiliate leading and supporting affiliate initiatives.
QUALIFICATIONS / EXPERIENCE REQUIRED:
Life science degree coupled with UK Regulatory Affairs (lifecycle) experience.
Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.
For a confidential discussion please telephone Christian Simon at AXESS Limited on 020 8560 2300.
To apply, please click APPLY ONLINE button.
Reg Affairs Project Manager / Regulatory Project Manager/ reg affairs jobs / careers / pharma regulatory project manager / London / Maidenhead / Reading / reg affairs officer / reg affairs manager / UK / South East / London
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