Hybrid Regulatory Affairs Senior Associate (Pharma)

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*** #J-18808-Ljbffr