Title: Regulatory Affairs Associate/Senior Associate (Contract)
Company Summary
A mid-sized biopharma company, in San Francisco, is looking to bring on a Regulatory Affairs Associate/Senior Associate to join their team, on a contract basis. You will play a key role in preparing and compiling regulatory submissions.
The Regulatory Affairs Associate/Senior Associate will be responsible for:
- Supporting clinical trial activities
- Reviewing investigatory document packages (FDA submissions)
- Managing queries with regulatory agencies
The ideal Regulatory Affairs Associate/Senior Associate should have:
- BS (in biology or physical sciences is a plus) with 2+ years' experience at the Associate level or 5+ years' experience at the Senior Associate level
- Relevant Regulatory Affairs experience in the pharma industry
- Experience with eCTD INDs
- Experience working with CROs
If you're interested in this Regulatory Affairs Associate/Senior Associate role, please don't wait to apply!
