Job Summary
A company is looking for an Assistant Director of Regulatory Affairs to join a biotechnology firm focused on life-threatening conditions.
Key Responsibilities
- Main point person responsible for writing INDs
- Spend 50-60% of time writing sections of IND with support from cross-functional teams
- Opportunity to manage a team member and gain people management experience
Required Qualifications
- Bachelor's Degree with 12 years, Master's Degree with 10 years, or PhD with 5 years of experience in biologic or pharmaceutical industries
- Must have IND experience as the point person, submitting in ECTD format through the ESG portal
- Experience in Regulatory Affairs within a pharmaceutical or biotech company
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