Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote

Requirements

• Based in the United Kingdom
• Minimum 2–3 years of experience in Site Activation, Study Start-Up, Regulatory Affairs, or Clinical Research
• Strong experience with site document collection, review, and submission preparation
• Experience supporting clinical trial regulatory submissions in the UK
• Experience performing ICF adaptations
• Solid understanding of site activation and study start-up processes
• Strong attention to detail and ability to manage multiple priorities and timelines
• Bachelor's degree in Life Sciences or a related field
• Fluent English communication skills, both written and verbal
• If this role sounds of interest, please apply today!
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• IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.