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    OL

    OLSA Resources, Inc.

    Manufacturing

    QA Specialist-28897

    IL-Waukegan, United StatesOn-SiteContractPosted 4w ago
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    Job description

    This position provides direct support to ACPRU Data Systems staff with regards to Phase 1 Clinical Research Studies conducted at the  Clinical Pharmacology Research Unit (ACPRU). Responsibilities include: review source documentation and facilitate discrepancy reconciliation, perform ECG Abbios reconciliation, verify hand entered/transcribed data, manage paper CRFs and other study related paper forms, support monitoring activities, communicate with the ACPRU staff to request corrections to source data or clarifications, maintain data review tracking log and other assigned duties requested.

    Candidates must know MS Word and Excel, and be able to learn a proprietary system quickly.

    Enter qualifications here

    Permanent Position, VERY competitive pay scale

    TO BE CONSIDERED FOR THIS POSITION IMMEDIATELY (Email ALL OF THE FOLLOWING as an attachment)
    1.) RESUME, (REQUIRED)
    2.) HIGH SCHOOL DIPLOMA or GED, (REQUIRED)

    3.) COVER LETTER, (REQUIRED)
    4.) Vaccination records of the last year TB AND HBV (IF YOU HAVE THIS)
    All applications failing to follow these instructions will be deleted BEFORE consideration.

    Job details are sourced from the employer's original posting.

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    About the company

    OLSA Resources, Inc.

    responsibilities effectively.

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    Industry
    Manufacturing
    Open roles
    657

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