Quotient Sciences in Nottingham seeks an experienced Regulatory Affairs Manager – Clinical Trials to lead regulatory submissions for early‑phase studies. You’ll work with MHRA, REC, HRA and ARSAC, guiding sponsors and internal teams from submission through approvals and reporting.
This flexible role offers onsite/hybrid/remote options, opportunities to mentor colleagues, and influence regulatory processes while expanding your expertise in UK clinical trial regulation.
Clinical Trials Regulatory Lead - Early-Phase in Nottingham employer: Quotient Sciences
At Arcinova, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the rapidly evolving field of mRNA manufacturing. Our commitment to employee growth is evident through comprehensive training programmes and opportunities to work alongside industry experts, ensuring that every team member can develop their skills while contributing to groundbreaking pharmaceutical advancements. Located in a state-of-the-art facility, our culture prioritises safety, quality, and continuous improvement, making it an ideal place for passionate scientists to thrive and make a meaningful impact.
