Consultant I, Medical Writing
Syner-GBTM Layout, BangalorePosted 20 days agoA free account shows the apply link for every role and matches you to the ones that fit your resume.
About the role
Syner-G provides biopharma product development and delivery consulting for clients across drug development and commercialization. The Medical Writing Consultant authors regulatory documents, coordinates client projects, and ensures submission-ready work aligned with regulatory standards.
What you'll do
- Author clinical study reports, protocols, and submission materials
- Develop complex regulatory modules and designation applications
- Apply quality control and submission-readiness processes
- Track project timelines and coordinate with clients
- Collaborate across teams to ensure document accuracy
- Contribute to regulatory strategies for early-stage clients
Skills
Must have
- Medical writing
- Regulatory writing
- Regulatory submissions
- Scientific content interpretation
- Project management
Tools
- Microsoft office
- Word
- Excel
- Powerpoint
- Teams
- Ms project
- Veeva vault
Who it's for
- Experience
- 3+ years
- Domain
- biopharma
About Syner-G
Syner-G has 2 open roles in Bangalore, at Syner-G Offshore Office, Commerce @ Mantri. See every Syner-G role.
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