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    Data Entry Associate - United Kingdom - Worldwide Clinical Trials

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    Description
    Pharmacovigilance Associate - UK - Office/Hybrid/Remote

    Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality.

    Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

    Why Worldwide
    Review incoming SAE data for completeness and accuracy. Perform QC of SAEs processed by other PV Associates
    Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
    Generate regulatory reports and perform safety submissions as needed. Good understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
    Good understanding of computer technology, and management of relational database systems, including extraction of data
    Bachelor's degree in a science-related field, nursing, or equivalent
    Minimum of 3 years of pharmacovigilance experience (pre-approval clinical trials)
    Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
    For more information on Worldwide, visit or connect with us on LinkedIn .
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