Job Summary
A clinical and scientific staffing company has an open position for a .
Candidates will be responsible for the following:
- Working with clients to develop regulatory strategies and plans for FDA
- Crafting, writing, and editing regulatory submissions
- Providing advice on drug development strategies
Must meet the following requirements for consideration:
- Scientific background and Bachelor's degree
- Demonstrate excellent communication skills
- Have strong early phase experience
- A high proficiency of FDA process, guidelines, and meetings
