R Dpartners is seeking a Site Activation Specialist to support start-up activities for clinical studies in the UK. You will work with cross‑functional teams to ensure smooth site activation, including regulatory submissions, document collection, and contract negotiations.
You must have the right to work in the UK. Key responsibilities include feasibility analysis, regulatory document collection, ethics submissions, and review of essential documents.
Site Activation Specialist (IVD) — Flexible Hours employer: R&D Partners
R&D Partners is an exceptional employer, offering a dynamic remote work environment that fosters collaboration and innovation in the pharmaceutical and biotech sectors. With a strong emphasis on employee growth, we provide ample opportunities for professional development and career advancement, all while supporting a culture of teamwork and excellence. Join us to be part of a forward-thinking organisation that values your contributions and prioritises your well-being.
