IQVIA is seeking a Country-level Site Activation professional to manage activation tasks for UK sites, working remotely with the SAM and project team. You will ensure regulatory readiness, maintain study documents, and monitor timelines in line with SOPs and ICH/GCP guidelines.
A background in life sciences and 3 years in clinical research are required. This home-based role requires strong knowledge of the UK clinical trial landscape and experience with regulatory submissions, ethics approvals,
Remote UK Study Start-Up Specialist – Clinical Trials employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
