
Senior Medical Writer
2 days ago
Role: Sr.Medical Writer
Location: Chennai/WFH
Shift: Rotational Shift
Senior Medical Writer for its Creative Communications team. In this role you will be responsible for:
Developing clear, concise, and scientifically accurate medical documents and marketing collateral, including presentations, whitepapers, video scripts, flashcards, brochures, and more.
Creating audience-appropriate medical content for patients, healthcare professionals, regulatory agencies, and internal stakeholders.
Conducting thorough research and literature reviews to ensure content accuracy and compliance with industry standards across all content formats mentioned above.
Collaborating with subject matter experts, scientists, and regulatory teams to develop compelling and compliant medical writing materials.
Adhering to client and regulatory guidelines (e.g., AMA, ICH, FDA, EMA) while ensuring consistency, accuracy, and scientific integrity in all documents.
Reviewing and revising content based on feedback from reviewers and editors.
Managing multiple writing projects simultaneously while meeting strict deadlines and quality standards.
Supporting quality control and peer-review processes to ensure excellence in medical
documentation.
Requirements for this role include:
A Bachelors, Masters, or Doctorate degree in Life Sciences, Medicine, Pharmacy, or a related field.
8+ years of experience in medical writing within the pharmaceutical, healthcare, or life sciences industries.
Strong understanding of medical and scientific terminology and regulatory requirements.
Excellent writing, editing, and verbal communication skills with a keen eye for detail and ability to editorialize medical content to engage multiple audiences.
Familiarity with industry guidelines (e.g., ICH, GCP, AMA, FDA, EMA).
Familiarity with the Veeva Vault Platform.
Team handling and project management experience is an added advantage.
Proficiency in Microsoft Office Suite and reference management tools.
Strong organizational skills, ability to multitask, and work independently under tight deadlines. Experience collaborating with cross-functional teams, including researchers, medical professionals, and regulatory expert
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