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Hyderabad, Telangana, India
Posted: Feb 22, 2025
On-siteFull-time
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Job Description
Skills:
Regulatory writing, "protocol design", "Clinical trails", "report writing", eCTD, regulatory submission, "ICF Preparation", CRF Review,

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
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Additional Info
Min. Experience
-
Job Location Type
On-site
Job Type
Full-time
Predicted Seniority Level
Mid-Senior level
Job Duration
-
Language(s)
All
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
Pharmaceutical Manufacturing
Job Function
Marketing, Public Relations, and Writing/Editing
Employer
Vimta Labs Ltd
Preferred Applicant Countries
India
Job Ref
J25DF1C7D0558
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