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Covance Norway is looking for Senior Clinical Research Associate! (hom - Oferta z Jobs.pl

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Covance Norway is looking for Senior Clinical Research Associate! (hom

Nr ref.: /JOBS.pl

  • At the moment we are looking for Clinical Research Associates (CRA) / Senior Clinical Research Associates (SCRA).

    Location: Norway (home based in Oslo area)

    Main Job Responsibilities:

    All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.
    Site administrating and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP;
    Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
    Completing Serious Adverse Event (SAE) reporting, processing production of reports;
    Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned;
    Interact with internal work groups to evaluate needs, resources and timelines;
    Assist with training, mentoring, and development of junior employees, e.g. co-monitoring;
    Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned.

    Candidate Requirements:

    Degree educated (Life Science)
    Few years of relevant clinical research experience in pharmaceutical or CRO industries
    Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
    Full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
    Excellent site monitoring skills
    Excellent study site management skills
    Excellent registry administration skills
    Ability to work with minimal supervision
    Good planning and organization skills
    Good computer skills with good working knowledge of a range of computer packages
    Excellent verbal and written communication skills
    Ability to resolve project-related problems and prioritizes workload for self and team
    Fluent Norwegian and English language skills

    Key Words:

    SCRA, CRA, clinical research associate, clinical research, monitoring, clinical trails associate, CRO, pharmaceuticals, clinical research organisation, Norway, Oslo,Drammen, CRAII, clinical study.


    Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.


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