SRG, on behalf of a global biopharmaceutical client, is seeking a Regulatory Associate – CTA to deliver global regulatory strategies for Clinical Trials. The role interfaces between global functions and affiliates to drive submissions, CTR processes and inspection readiness.
The position requires 5–6 years CTA experience, strong IT skills (Word/Excel/PowerPoint/Adobe Acrobat), and fluent English in a matrix, cross‑cultural environment. Hybrid role based in Maidenhead.
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Global CTA Regulatory Specialist – Clinical Trials 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.
