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.