Create a Job Alert.

Enter your email below to save this search and receive job recommendations for similar positions.
Thank you. We'll send jobs matching these to
You already suscribed to this job alert.
No Thanks
What job do you want?

Senior Regulatory Affairs Consultant job in London at Wentworth Life Sciences

Create Job Alert.

Get similar jobs sent to your email

Apply to this job.
Think you're the perfect candidate?
Apply on company site

You’re being taken to an external site to apply.

Enter your email below to receive job recommendations for similar positions.
Senior Regulatory Affairs Consultant at Wentworth Life Sciences

Senior Regulatory Affairs Consultant

Wentworth Life Sciences Europe Full-Time
£60,000 - £80,000 / year
Apply on company site

Create Job Alert.

Get similar jobs sent to your email

Do you have significant experience in the regulatory affairs field? I am looking for a senior professional that is looking to take the next step in their career, working on gene editing, cell and gene therapy and vectors as well as ultra orphan diseases!

I have a vacancy with a leading consultancy to join the team on a permanent basis. This role can be based anywhere in EUROPE.

You will lead multiple MAA's and BLA's at EU level and lead the regulatory strategy in these for your clients.

As a Senior Regulatory Affairs Manager/Consultant, you will be responsible for tasks and activities including:

Providing clients with regulatory consultancy services regarding biologics / clinical development programs through to marketing authorisation and post marketing support.

Drafting, preparation and review of documentation for regulatory submissions such as (IMPD/IND/MAA/BLA, PIP, ODD), scientific advice briefing documents and applications for orphan designation

Participation in due diligence activities as part of business development and investment activities by clients

Contribution to regulatory strategies for client activities.

Supporting clients as a subject matter expert

Management and delivery of client projects using internal resources, participating in client and agency meetings. Ensuring assigned client projects meet timeline commitments.

Client relationship management, including oversight of project plans and timelines, budgets and deliverables

Company representation at external conferences, including the provision of training workshops

Business development activities (e.g. identifying opportunities for work, new client meetings etc.)

Supporting and advising the wider group projects as required. 

Requirements :

To be successful in this position you will preferably have an advanced degree (minimum masters) in a relevant life science discipline and must have at least 4-5 years’ experience in a focussed role in the biotech / biopharmaceutical industry or regulatory consultancy industry.

In-depth experience in regulatory affairs and an in depth understanding of regulatory requirements of a range of activities for biological products during development.

Apply now to find out more about the job or contact Isabel Brickle at Wentworth Life Sciences for more information on the position

Recommended Skills

Business Development
Pre Clinical Development
Biologics License Applications (Bla)
Customer Relationship Management
Apply to this job.
Think you're the perfect candidate?
Apply on company site

Job ID: 213498906


For your privacy and protection, when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. Learn more.

By applying to a job using you are agreeing to comply with and be subject to the Terms and Conditions for use of our website. To use our website, you must agree with the Terms and Conditions and both meet and comply with their provisions.