Senior Regulatory Affairs Associate

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Regulatory Affairs Associate based in India. This role offers the opportunity to lead the planning, coordination, and execution of clinical trial submissions across multiple countries and regulatory environments. You will manage Clinical Trial Applications (CTAs) from end to end, ensuring submissions are timely, accurate, and compliant. Working across EU CTR and Rest of World (ROW) requirements, you will navigate complex regulatory landscapes and proactively manage risks and dependencies. The position involves close collaboration with global clinical, regulatory, and operational teams. You will also build strong stakeholder relationships, monitor submission performance, and drive quality improvements. This is a high-impact opportunity to contribute to the efficient advancement of clinical development programs and, ultimately, therapies that benefit patients.

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