Regulatory Affairs Lead/Head of Department - England, United Kingdom - Clinical Professionals Limited

Description

Regulatory Affairs Lead/Head of Department

Job Type:
Permanent

Regulatory Affairs Lead/Head of Department

An opportunity to work as a Regulatory Affairs Lead for a growing pharmaceutical company that specialise in generic, OTC, and prescription medicines.

The business is increasingly growing and is looking for an experienced leader who is personable, detail-oriented, and successful in driving regulatory strategies.

The position will work with other functions such as medical and PV supporting the business where needed. Full management of the UK product portfolio, MAA submissions, all deficiency responses, technical transfers, and all post-approval activities.

• Responsible for all in-licensing and out-licensing projects.
• Financial oversight of project costs and departmental budgets.
• Management of all external consultants and service providers.
• Management mentoring and training of all regulatory staff.
• Management of all pharmacovigilance and medical information activities
• Regulatory intelligence monitoring, attending relevant conferences/seminars and scientific advice meetings.
• Full liaison with commercial and launch management teams

Scientific degree/life sciences degree with a minimum of 8 years' experience in Regulatory Affairs.

• Excellent people skills and can influence decisions at a senior level.
• Detail drive, strategic, personable, and knowledgeable about the UK regulatory environment.

An excellent opportunity to step into a lead regulatory role and influence key decisions at a senior level, the role offers great flexibility and a chance to drive the regulatory functions for a growing business.

To be considered for this role you MUST have previous experience working at a senior level and have previous experience leading a team and driving RA strategy.