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5 - 10 years
5.0 - 10.0 Lacs P.A.
Hyderabad
Posted:2 months ago| Platform: 
Work from Office
Full Time
Urgent Opening for Senior Medical Writer @ Vimta Labs Ltd, Cherlapally, Hyderabad. Experience: 5-10 years of experience in protocol design for Clinical trials, PK/PD study design for biosimilars, ICF preparation, CRF/eCRF review Responsibilities: Experience in protocol design for Clinical trials, PK/PD study design for biosimilars, ICF preparation, CRF/eCRF review Well versed with study report writing and eCTD requirement for regulatory submission. Have to work closely with Statistician for data analysis and study results review. Handle sponsor, regulatory and ethics committee queries. Other regulatory writing experience will be an added advantage. Interested candidates can share their resumes to keerthana.rojanala@vimta.com Contact: Keerthana 9160712930
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