9 Medical Writer jobs in India available for remote work from home. Apply for positions such as Medical Writer, European Senior Medical Writer, Senior Medical Writer Medical Information and more! Discover the best work-from-home or hybrid, full- and part-time jobs.
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The primary role involves developing accurate, high-quality, and compliant medical and scientific content based on clinical data, publications, and medical insights. This includes creating various materials like slide decks, manuscripts, and medical information pieces while ensuring scientific accuracy and adherence to standards.
Develop, review, and adapt medical content for European markets to support product launch activities across various formats. Collaborate with cross-functional teams to ensure scientific accuracy, regulatory compliance, and cultural alignment for HCPs and patients.
The Senior Medical Writer will develop high-quality scientific and medical materials while providing mentorship and strategic guidance to the writing team. They will also build strong relationships with international pharmaceutical clients and key stakeholders to ensure scientific accuracy and effective data dissemination.
The Medical Writer II performs end-to-end scientific writing, including managing publication plans and ensuring documents are MLR-ready for submission. They also mentor less experienced writers and collaborate across departments to ensure document accuracy and regulatory compliance.
The Medical Writer II manages end-to-end scientific writing workflows, including publication planning, journal submissions, and congress activity coordination. They ensure accurate documentation and adherence to regulatory standards while providing operational support to cross-functional teams.
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The Medical Writer II manages end-to-end scientific writing workflows, including publication planning and Veeva Vault document management. They also mentor less experienced writers and ensure all deliverables meet regulatory and client standards.
The Senior Medical Writer will author, review, and manage clinical and regulatory documents to support global drug development programs. They will also coordinate cross-functional reviews and serve as the primary medical writing representative on project teams.
Develop high-quality scientific materials including manuscripts, posters, and abstracts while ensuring strategic alignment and scientific accuracy. Lead and mentor a team of scientific writers and maintain professional relationships with pharmaceutical clients and key opinion leaders.
Develop, review, and adapt medical content for regional and international markets to support product launch activities. Collaborate with cross-functional teams to ensure scientific accuracy and compliance with regional regulations.
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