Regulatory Affairs Senior Associate

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***