Regulatory Affairs Leader job in Reading, England

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First Name*

Last Name*

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Are you an employer or a jobseeker?*

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

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Job type: Permanent

Discipline: Project Manager

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

Proclinical has partnered with a global pharmaceutical organisation in search for a Regulatory Affairs Project Manager. In this role will be responsible for leading projects throughout the regulatory lifecycle

Job Responsibilities

Whilst strategic development will be involved, the role requires a more hands on project management focus
You will be expected to ensure cross-functional teams, partners, stakeholders, etc deliver their part of regulatory projects
You will focus on global oncology studies throughout the entire regulatory lifecycle
Review labelling, pack leaflets and summary of product characteristics etc. to ensure compliance with current legislation and registered particulars and act, as agreed with supervisor, to secure regulatory approval where necessary

Skills and Requirements

Life sciences or chemistry degree with proven relevant experience within regulatory in the pharmaceutical industry (country affiliate role for UK & Ireland
Prior project focused regulatory experience across various global markets is essential
Strong communication skills are essential and prior experience managing third-party/ CRO relationships is strongly desirable
Oncology experience is preferred though not essential

To Apply

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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