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    Job · 15378745

    cliantha research ltd logo

    Doctor

    cliantha research ltd · Ahmedabad · onsite · Posted 49d ago

    Undisclosed1–2 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Role & responsibilities


    • Efficiently planning and executing the logistics of all clinical studies.

    • Responsible for overall conduct of the bioavailability bioequivalence clinical studies under supervision.

    • Responsible for selection of the participants in the trial, safety of the subjects, operation of the clinic, communication with the sponsor, ethics committee and study team.

    • Responsible for screening of the participants in the trial and monitor the day to day activities of the study team.

    Job Location: Ahmedabad


    Required Qualifications/ Experience:


    • MBBS degree from a recognized institution
    • Valid Medical Registration Certificate
    • 1-2 years of experience in conducting and managing Bioavailability (BA) and Bioequivalence (BE) studies.

    Sourced from naukri

    Skills

    clinical researchclinical trialsICH-GCPClinical OperationsbioequivalenceBioequivalence Studies

    About Cliantha Research

    cliantha research ltd logo

    cliantha research ltd

    Clinical Research

    894

    employees

    2004

    22 years old

    Ahmedabad, Gujrat

    India

    ₹4.8L PA avg

    Avg at Cliantha Research

    About

    Cliantha Research is a Clinical Research Organization offering comprehensive services aimed at ensuring regulatory compliance in clinical trials across various therapeutic areas.

    Industries

    Clinical ResearchBiotech & Life sciencesAnalytics & KPO

    Employee ratings

    10 reviews

    4.1/ 5

    Culture

    3.6

    Career growth

    3.2

    Work-life

    3.9

    Employees rate it well for

    Job Security44Overall Company41

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    Doctor · waiting for your command