Principal Medical Writer
Skills
Clinical DataClinical Data ManagementClinical TrialsData PresentationDrug DevelopmentInternet ExplorerMedical Review
What the job involves
The main requirements, responsibilities and hiring steps.
Requirements
- 5-6 years of experience in regulatory medical writing
- Master’s degree in natural sciences preferred or strong candidates with a Bachelor degree
- Thorough understanding of the drug development process and clinical data management
Nice to have
- Medical Writing
- Drug Development
Day to day
- Acts as the medical writing expert for assigned drug projects
- Leads the development of the project level data presentation strategy and messaging standards
- Independently authors submission documents and collaborates closely with the team