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informed consent medical writing csr study protocols dsur📋 Description
- Assists in developing and reviewing CSR, study protocols, IC, and IB.
- Supports safety reports (PBRERs, DSURs, etc.).
- Conducts literature scans and prepares summaries and reports.
- Proactively incorporates team input into edits and revisions.
- Performs quality review and verification against source data.
- Completes WI, process guidelines, and SOP trainings per schedule.
- Contributes knowledge on the Medical Device arena.
- Streamlines clinical research writing to present data coherently.
🎯 Requirements
- Allied health professional (MD, Nurse, or Pharmacist).
- Strong medical terminology and anatomy knowledge.
- Experience in copy review.
- Project management.
- Experience in supporting medical device or pharma.
🎁 Benefits
- Daily Meal Subsidy
- Flexible working hours and work from home privileges.
- HMO coverage up to 2 dependents subsidy
- Life and accident Insurance
- 15 Sick Leave and 15 Vacation Leave
- Monetized leave
- Performance Based Annual Salary Increase
- Clothing Allowance
- Rice Allowance
- Laundry Allowance
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