Job Summary
A company is looking for a Scientific Writer to draft and manage submission documents for nonclinical pharmacology.
Key Responsibilities
- Collaborate with scientists and regulatory teams to develop data packages for drug candidates
- Independently author and manage reviews of nonclinical study reports and submission documents
- Drive document approval processes and participate in process improvements for scientific writing
Required Qualifications
- BS or MS with 6+ years of experience, or PhD in a Life Sciences-related field with 2+ years of relevant experience
- Experience with eCTD and the drug development process
- Proficiency in computer applications such as Word, Excel, Adobe, and GraphPad Prism
- Fluency in the English language
- Passion for science and teamwork
Comments