PE Global are currently recruiting for a Regulatory Affairs Senior Associate for a 12 month contract role with a leading multinational Pharma client based in Uxbridge – hybrid.
Job Responsibilities
- Execute the regional regulatory strategy and regional regulatory plans.
- Prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications, marketing authorizations, and lifecycle management activities.
- Use of Amgen systems and document management.
- Ensure and support regulatory product compliance.
- Work with Policies and SOPs.
- Build effective relationships and communication paths across local and functional organizations.
- Enable efficiencies and seamless execution across the region countries.
Requirements
- Ideal candidate has 3 – 4 years’ experience who has mix of clinical trial lifecycle knowledge and post marketing product experience.
- Experience in Viva Vault (RIM).
- Oncology experience is desirable.
Interested candidates should submit an updated CV.
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***
Contract 
Uxbridge, Middlesex, UK 
42032596 
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