Description
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 [email protected]
Contact:
Keerthana
9160712930
Role: Medical Writer
Industry Type: Clinical Research / Contract Research
Department: Research & Development
Employment Type: Full Time, Permanent
Role Category: Pharmaceutical & Biotechnology