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Pharmacovigilance Internship

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

Posted: 2019-05-10

Job Description
Job Description:

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

    RESPONSIBILITIES:

    Attend Investigators Meeting.
    Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory guidelines.
    Ethics Committee Submission
    Help in preparation of Regulatory Binder.
    Maintain updated Site Files and collection of the essential documents and project related documents during the site visits and maintain Central Clinical File.
    CRF retrieval as per the project instructions.
    Coordinate and distribute Clinical Study Material to study sites.
    Archival of study documents.

    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
    Rani

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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