Medical Writer (Creative Writing) | FINJO N990

Medical Writer

Location : RRD - Chennai ( Work from Office)

No of positions : 2

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 Bachelor’s, Master’s, 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, clinical research processes, 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 experts.