Senior 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 Senior Medical Writer based in India. This is a strategic opportunity for an experienced medical writer specializing in clinical trial disclosure and transparency. You will lead complex disclosure projects from initiation through delivery, helping global clients meet evolving regulatory requirements. The role combines advanced medical writing, regulatory interpretation, clinical document review, and client consulting. You will work across submissions such as protocol registrations, results postings, plain language summaries, anonymization packages, and CCI justification documentation. Your expertise will directly support transparency, data protection, and patient access to meaningful clinical trial information. You will also contribute to process improvements while mentoring junior colleagues and raising quality standards across the team. The position is well suited to a detail-oriented professional who can navigate complex regulations while communicating clearly with both technical and non-technical stakeholders.