Sas/clinical Research/pharmacovigilance @ Resolve GROU OF

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Sas/clinical Research/pharmacovigilance

Resolve GROU OF
0 - 0 yrs
Hyderabad
7 years ago
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Desired Candidate Profile

Overall responsibility for study management, responsible for monitoring of studies in accordance to protocol/ SOPs/ Guidelines.

RESPONSIBILITIES:

Track all adverse event reports received and completed
Review and assess all source documents, and compile data in an adverse event report
Data enter report into the client safety database
Code adverse events in the client safety database
Release report to client through client safety database.

Education :Msc., lifescience,nursing , B.Pharmacy/M.Pharmacy/ PharmD, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, etc.) and lifescience graduates.

For details

VIJI

Education:

UG: B.Pharma - Pharmacy, B.Sc - Any Specialization, Bio-Chemistry, Biology, Microbiology, Nursing, Optometry, Zoology, BAMS - Any Specialization, Ayurveda

PG: M.Pharma - Pharmacy, MS/M.Sc(Science) - Any Specialization, Bio-Chemistry, Biology, Microbiology, Nursing, Optometry, Veterinary Science, Zoology, MVSC - Veterinary Science

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Write briefly about yourself, your experience and education (*)

Attach ResumeMax 2.38 MB (RTF, PDF, DOC, DOCX formats only parsed)

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Resolve GROU OF

Resolve GROUP OF COMPANIES Resolve is a leading global research organization providing comprehensive, integrated drug development, laboratory management services. Our clients and partners include pharmaceutical, biotechnology, medical device, and academic and government organizations. Resolve ap...

Sas/clinical Research/pharmacovigilance @ Resolve GROU OF

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