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Clinical Research/ Pharmacovigilance jobs -For Fresher

Keywords / Skills : molecular biology, biotechnology, biochemistry, zoology, microbiology, biotech, nursing, pharmacy, biomedical, pharmacovigilance, clinical research, clinical data management

Posted: 2019-06-13

Job Description
Job Description:
    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.

    Call for further details
    8754205710

Desired Candidate Profile
    Please refer to the Job description above


About Company

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 applies innovative research, therapeutic expertise and a firm commitment to Pharma companies and time curve of drug development and optimize value in delivering life-changing therapies, drugs to improve health.
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