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Posted on 21 Jul, 2024
Overview
- Industry - CRO, Clinical Research Organization
- Functional Area - Research / R&D - Pharma / Medical / Health / Biological Sciences
- Job Role - Other Top Management R&D / Research - Pharma / Medical / Health / Biological Sciences
- Employment type - Full Time - Permanent
- Work Mode - In Office
Job Description | Role and Responsibilities
- You'll write and review documents for clinical trials, making sure they're accurate, meet regulations, and explain things clearly.
- You'll collaborate with other experts to ensure all the information is there and makes sense.
- You'll interpret complex data from studies and scientific literature, then explain it in a way that's easy to understand.
Candidate Profile | Who Can Apply
Education
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
About Employer
Contact Details
Email - contact@msclinical.com
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