Regulatory Affairs Associate
Role Overview
The Regulatory Affairs Associate supports the preparation, submission, and maintenance of regulatory documents for pharmaceutical products.
The associate works closely with various stakeholders including regulatory, quality, clinical, and technical teams, to assist in keeping submission materials accurate, organized, traceable, and ready for review.
This role is suited to a recent graduate with relevant internship or co-op experience in regulatory affairs or pharmaceutical quality.
Full Job Posting
Preferred qualifications
- Hands-on exposure to FDA submission support, or IND documentation.
- Experience with Veeva RIM, Veeva QualityDocs, or similar systems.
- Experience reviewing controlled documents, maintaining traceable electronic records, analyzing quality or regulatory trends, or presenting findings to colleagues.
About Verastem Oncology
Public biopharmaceutical company developing and commercializing small-molecule medicines for patients with RAS/MAPK pathway-driven cancers.
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