• US-CA-SanDiego: Clinical Research Associate

    From http://biotech.fyicenter.com@21:1/5 to All on Fri Oct 16 11:08:21 2015
    US-CA-SanDiego: Clinical Research Associate
    To apply for this position, please visit this Website. http://biotech.fyicenter.com/jobs/99886637_Clinical_Research_Associate_.html Date: 16-Oct-2015
    To see other BioTech job opportunities, please visit http://biotech.fyicenter.com/

    Clinical Research Associate

    Duties and Responsibilities

    Leads development of site and study documentation such as training materials, reports, consent documents, study operation manuals, monitoring plans and regulatory submissions for the screening, initiation, conduct and reporting of clinical trials. Leads
    preparation and maintenance of manuals, forms, tracking tools and reports for AE reporting, medical monitor review, CEC and DSMB conduct, as well as liaison with committees and members for scheduling and documentation. Lead development of department SOPs
    and work instructions, support departmental planning. Generates clinical data and status reports to support management, project team, study reports, regulatory submissions and publications.

    Coordinates and prepares clinical study protocols with expert input (such as MD, statistical).

    Supports investigational device administration including all documentation for forecasting, shipping, receiving, disposition, complaints, and returned goods. Supports clinical data management in CRF development, validation rules and other reporting and
    analysis tasks, reimbursement for sites. Communicates with team and department members. Supports and maintains documentation of all clinical research activities, e.g. site communications, correspondence, inventory information. May support project teams
    for product development. Support department activities as required.

    Minimum Qualifications, Knowledge, Skills and Abilities

    Working knowledge of and ability to follow US FDA regulations, ISO 14155, Good Clinical Practice and Japanese regulations. Follows established SOPs and work instructions. Experience in clinical research protocols, reporting, regulatory submissions,
    development of monitoring/analysis/data management plans with technical support. Advanced knowledge of clinical research methods and practices for medical devices, including IDE and CE Mark studies. Advanced auditing and self-auditing skills Working
    project management and vendor management skills Advanced clinical data monitoring skills: paper and EMR Excellent/advanced oral and written communications skills Proficient computer skills including word processing, spreadsheet generation and database
    querying and reporting skills. Ability to be point of contact for investigators and site staff on a clinical trial. Demonstrable skills in organizational and project administration skills, tracking study activities for timeliness and completeness. BS
    degree in life science, nursing or equivalent 8+ years directly related work experience or equivalent

    Thank you,
    BioTech FYI Center

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