Principal Regulatory Medical Writer

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Principal Regulatory Medical Writer based in India.

This role offers the opportunity to lead the creation of high-quality regulatory and clinical documentation that supports the development and approval of innovative healthcare products.
The position requires advanced scientific writing expertise, strong knowledge of regulatory standards, and the ability to manage complex deliverables across multiple therapeutic areas.
You will collaborate with cross-functional teams including clinical operations, regulatory affairs, data management, and subject matter experts.
The role combines independent ownership, strategic client partnership, and technical leadership within a global healthcare environment.
You will contribute to improving patient outcomes by ensuring accurate, compliant, and impactful communication of scientific and clinical data.
This opportunity is ideal for experienced medical writers who enjoy mentoring others, solving complex challenges, and driving excellence in regulatory submissions.