Regulatory reputed company I
Master's in reputed company/life science or communications required; 1+ year medical/regulatory/clinical writing experience; ability to reputed company and edit FDA and ex-US regulatory submissions (eCTD), interpret clinical data, and manage timelines.
Key Responsibilities
- authoring submissions
- editing documents
- tracking milestones
Skills & Tools
eCTD
Job Details
- Category: Research and Development (R&D)
- Seniority: Entry Level
- Commitment: Full Time
- Workplace: Remote — reputed company
- Languages: English
Benefits
- 401k matching
- Generous reputed company time off
- Retirement plan
- Generous parental leave
About Ora
A full-service ophthalmic drug and device development firm guiding clients through clinical research to bring therapies to market. — Industry: Research and Development
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