Job Summary
A company is looking for an Associate Director, Medical Writing (Remote).
Key Responsibilities
- Develops and drives messaging strategy for clinical programs to ensure effective communication and consistency across documents
- Aligns and coordinates information across clinical program documents, ensuring accuracy and support by appropriate data
- Sets program-level standards and oversees the delivery of high-quality medical writing deliverables for regulatory submissions and publications
Required Qualifications
- BA/BS or higher with at least 6 years of writing experience in the pharmaceutical industry
- Solid understanding of the clinical development process and associated documentation
- Expertise in MS Office, particularly in word processing and document formatting
- Knowledge of ICH and CTD guidelines for clinical and regulatory submissions
- Experience leading complex clinical or regulatory writing projects
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