Verbatim Pharma is seeking a Regulatory Affairs Manager to join their Global Clinical Trial Services team in a hybrid UK role. You will develop regulatory intelligence, craft regulatory plans, and provide project-based support, leveraging a solid grasp of EU directives, US CFR, and GMP/GDP regulations.
You will operate within a close-knit regulatory team, contributing to continuous improvement and ensuring compliance across global trials in a pivotal, patient-focused environment.
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Global Regulatory Affairs Lead — Hybrid (Clinical Trials) employer: Verbatim Pharma
Verbatim Pharma is an exceptional employer that prioritises a supportive and collaborative work culture, allowing Senior Recruitment Consultants to thrive in a fully remote environment. With a focus on personal development through tailored training opportunities and an industry-leading commission structure, employees can enjoy a fulfilling career while achieving a healthy work-life balance, including the unique benefit of unlimited holiday. Join a family-oriented team that values relationships and encourages you to excel without the pressure of unrealistic KPIs.
