Posted:9 hours ago|
Platform:
Work from Office
Full Time
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.
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).
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
Williams Lea
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