SRG seeks a Regulatory Associate to provide global regulatory expertise for Clinical Trials. You will be the primary interface between global functions and affiliates to deliver regulatory strategies, operations and outcomes with a focus on CTAs and EU CTR submissions.
You will collaborate across cultures in a matrix environment, manage timelines, and support inspection readiness while ensuring compliant processes and effective communication in English.
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Global Regulatory Associate – Clinical Trials in Maidenhead 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.
