Related skills
informed consent clinical study reports study protocols dsur investigator's brochureπ Description
- Assists in developing/reviewing clinical study docs (CSR, protocols, IC, IB, safety plans)
- Conducts literature scans/reviews for summaries/reports
- Incorporates team input into edits and revisions
- Performs quality review and verification vs source data
- Completes project/work instructions, process guidelines, SOP trainings
- Contributes knowledge on Medical Device topics
π― Requirements
- Allied health professional (MD, nurse, or pharmacist)
- Well-versed in medical terminology and anatomy
- Experience in copy review/copyediting
- Strong project management skills
- Experience in medical device or pharma sectors
π Benefits
- Daily Meal Subsidy
- Flexible hours and work-from-home privileges
- HMO coverage for dependents
- Life and accident Insurance
- 15 Sick Leave and 15 Vacation Leave
- Monetized leave
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