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Jobs Available : Clinical Research Associate

September 18, 2005 by administrator

Responsible for conducting bioequivalence & Bioavaliability studies. Responsible for writing protocols for Clinical Trials, Bioequivalence Studies, designing case record forms. Training of personnel on good clinical practices and standard operating procedures. Updating regulatory guidelines for Bioequivalence and Bioavaliability studies & all other related activities

Desired Profile:
MSc / M.Pharma
Should possess good analytical & drafting skills.

Bioserve is an upcoming CRO offiering BA / BE studies for national and international pharmaceutical organizations. Bioserve is committed to quality and cost effective services without compromising in ethical and regulatory requirements.

E-Mail Address (to send cover letters and resumes directly):info@bioserve.co.in

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