Medical Writer - Vimta Labs Ltd, Cherlapally.

Experience: 2- 6 years

CTC: As per market standards.

• 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