On-site
Part Time
To develop high-quality scientific content and documentation across therapeutic areas by conducting indepth literature reviews synthesizing data and delivering clear accurate and audience-appropriate materialsThe role involves contributing to both short and long term projects in the consumer healthcare and pharmaceutical sectors including medical safety preclinical clinical, regulatory educational and promotional contentAdditional responsibilities include editing proofreading reviewing referencing and verifying content to ensure adherence to high medical writing standardsThe role ensures timely delivery of project milestones while maintaining quality compliance and business value
M-Pharm, MSc, PhD
WNS
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