I am working with a CRO serving the pharmaceutical and biotechnology industries in the areas of clinical operations, pharmacovigilance, data management and regulatory submissions, looking to add an experienced medical writer to their team.
If you have strong written communications skills and are looking for a Medical Writer II position, please see the responsibilities and requirements below:
- Write clinical development plans, clinical study protocols, clinical study reports, and more!
- Develop and write INDs, NDAs and other regulatory submission documents
- Prepare annual reports and briefing documents for regulatory submissions
- Minimum of 5 years of medical writing experience
- Strong knowledge of the biotechnology/pharmaceutical industry and terminology
- Experience in aspects of drug development, clinical trial monitoring and data management