Job designation - Senior Associate(Regulatory Affairs)
Job Description - To Review, Process and Quality check Clinical Data Reports (CDRs) as per clinical guidance and submitting to the Regulatory Authorities as per timelines for the approval.Processing all kinds of Clinical reports like clinical study reports, Protocols and Amendments, Informed Consent Forms, Investigator's Brochure, IND, IMPD, etc by adhering GCP/ICH Guidelines.
Requirments -Any UG/ PG Graduate in any SpecializationWith 1-3 years of experience
Contact : aishwarya.p@saakiandargus.com
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