06 October 2008

Regulatory Associate

job designation-Regulatory Associate
job description-Prepares and submits regulatory documents to DCGI, including original clinical trial applications and amendments,Coordinates assembly, collection, and/or distribution of components of regulatory documents (e.g., appendices for clinical study reports, site regulatory documents, CRFs for regulatory submissions, meeting requests, etc.)Publishes (i.e., prepare) paper and electronic versions ofClinical study documents (including protocols, protocol amendments, clinical study reports, investigator brochures, etc)
job requirements-BSC in life sciences,1-3 years experience in regulatory affairs
contact-roochi, clinysis clinical research,
Address
C-46, Sec 62
Noida
Noida,U.P,INDIA 40153
Telephone:
91-0120-91204304600

No comments:

Post a Comment