IQVIA, a global leader in clinical research services, seeks an experienced Freelance Site Activation Specialist based in the United Kingdom to support start-up and site activation activities. You will collect and review UK regulatory documents, adapt ICFs, and coordinate submissions with investigative sites and internal teams to meet project timelines.
The role requires 2–3 years in site activation or regulatory affairs, a Life Sciences degree, and fluent English.
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Remote UK Site Activation & Submissions Specialist in Oxford 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.
