Associate

    HCL Technologies Ltd.
    San diego, CA
    Full-time, Part-time
    Similar jobs pay $11.00 - $16.60

    Job Description

    Responsible to work on Clinical study reports, Investigator's brochure, Protocol development and Clinical Evidence Summaries (1.) Developing Protocol, Investigator`s Brochure, Informed Consent forms, interim reports, Clinical Evidence Summaries and Clinical study reports (2.) To perform tasks including researching Medical information, summarizing data from clinical studies, consulting, editing statistical and clinical reports (3.) Review of Medical journals and technical reports (4.) Review Protocols, CRF`s, ICF`s and miscellaneous study documentation (5.) Working closely with Doctors, researchers and various people in Medical services to provide information which is accurate and easy for others to understand

    Experience

    >11 Years

    Qualification

    B.Pharma
    B.Tech
    Bachelor of Arts
    BASc - Bachelor of Arts and Science
    MBBS

    No. of Positions

    2

    Skill (Primary)

    Technical Domain skills(ERS)-Clinical-Clinical Operations

    Country

    USA

    Employee Group

    Contract

    City

    San Diego

    Entity

    CSW

    Auto req ID

    676585BR

    Removal Date

    05-May-2021

    Posting ID: 556732807Posted: 2020-05-22

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