0 - 4 years
4 - 8 Lacs
Posted:2 weeks ago|
Platform:
Work from Office
Full Time
Understand complex client briefs quickly and develop fit-for-purpose SLR protocols
Execute and/or oversee screening, data extraction, quality assessment, and synthesis
Ensure adherence to PRISMA guidelines and best practices
Validate and QC deliverables prepared by internal teams; identify and resolve gaps
Summarize findings in a structured format for publication or internal use
Provide support in publication planning, writing, and submission
Coordinate with cross-functional stakeholders, including medical writers, analysts, and project managers
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