Regulatory Affairs Associate
Location: United States
Position Type: Full-time
Job Duties:
- Prepare, review, and file clinical trial applications and marketing applications to the
international health agencies;
- Ensure submissions comply with applicable regulations and guidance documents;
- Advise clients on changing regulations and compliance requirements; and
- Track submissions and ensure timely filing of documents.
Qualifications:
- Bachelor’s degree in Life Sciences or a related field;
- 2-4 years of experience in regulatory affairs; and
- Hands-on experience preparing and submitting regulatory documents is preferred.
Travel: None
To apply for this position, send your resume to: hr@medpace.com
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