SRG in London is seeking a Graduate Regulatory Writer to begin a career in regulatory affairs within a global healthcare environment. The role provides hands-on experience in preparing regulatory documents used throughout drug development and submissions to health authorities worldwide.
Working in a cross-functional setting, you will collaborate with Regulatory Affairs, Clinical Development, Statistics and Drug Safety, develop scientific writing skills, and contribute to project plans while
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Graduate Regulatory Writer — Hybrid London (12-Month) employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
