Regulatory Affairs Manager in Uxbridge or Cambridge

6 days left

26 Jun 2019
23 Jul 2019
Contract Type
Full Time
Mary Bolt at CK Group is recruiting for a Regulatory Affairs Manager, to join a world leading pharmaceutical company at their site based in Uxbridge or Cambridge on a Permanent basis.

The Company:
Our client are at the forefront of providing the oncology and haematology communities with novel therapies that have changed patients' lives. They are known as an innovator who are consistently pushing the boundaries of science and have a rapidly expanding pipeline.

The Location:
Located less than an hour away from London by train, the role will be based in Cambridge or Stockley Park.

Cambridge is one of Britain's most beautiful cities, it still remains at the forefront of science and is one of Europe's most important biotechnology clusters.

Stockley Park was the UK's first and most successful business park. It has excellent transport links with the M4 and M25 motorways and Heathrow Airport few minutes away and a choice of railway and tube stations and extensive bus networks.

The Role:
The main purpose of the role will be to:
- Plan and manage regulatory submissions (e.g. clinical trial and marketing applications) and implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements.
- Provide regulatory guidance on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, Fast Track, compassionate use and paediatric plan) and direct the development of the regional product label by collaborating with the Labeling Working Group.
- Develop and/or implement innovative and compelling regulatory strategies designed to enable patient access and the lead development of regional regulatory documents and meetings in accordance with the regulatory strategy.

Further responsibilities will include:
- Directing the development of the regional product label by collaborating with internal stakeholders to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent.
- Managing regional label negotiation activities.
- Identifying and mitigating regulatory risks and support contingency planning.

Your Background:
To succeed in this role, you will come from a background in:
- Educated to degree level or above in life science or a related field.
- Significant Regulatory Affairs experience including an understanding of the registration procedures in region for MA, post approval changes, extensions and renewals as well as national registrations and an In-depth understanding of the drug development process from a Regulatory perspective.
- Excellent communication skills and experience of Health Authority interactions and needs of internal and external stakeholders as well as cultural awareness to achieve results internationally.

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference 45872 in all correspondence.