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    Clinical Research Associate - South San Francisco, United States - Centivax

    Centivax
    Centivax South San Francisco, United States

    2 days ago

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    Description

    Job Description

    Job Description

    Responsibilities:

    • As a vital member of our clinical team, the Clinical Research Associate will be responsible for conducting Phase I-IV single or multi-center studies in adherence to Federal Regulations and ICH guidelines.

    Key responsibilities include:

    • Collaborating with senior staff in planning study conduct.
    • Designing case report forms (CRFs) and managing Contract Research.
    • Organization (CRO) selection.
    • Selecting and training investigator sites, planning and organizing study meetings.
    • Evaluating, selecting, and training new study investigators.
    • Writing and assembling submissions related to study protocols.
    • Monitoring investigational sites to ensure protocol adherence.
    • Ensuring timely enrollment of patients and retrieval of CRFs from study sites.
    • Processing CRFs, including data cleanup and classification of data.
    • Completing study summaries and reports.

    Experience:

    • The ideal candidate should possess a minimum of 2 years of experience in clinical research monitoring.

    Key qualifications include:

    • Proven experience in the successful execution and monitoring of clinical trials.
    • Familiarity with Federal Regulations and ICH guidelines.
    • Strong attention to detail and organizational skills.
    • Ability to work effectively within a collaborative team environment.
    • Experience with vaccines against infectious diseases clinical trials highly desired but not absolutely necessary.

    Education:

    • A minimum of an Associate degree is required, but preference will be given to candidates with a Bachelor's degree.
    • Additionally, candidates should have at least 2 years of monitoring experience with preference on vaccines against infectious diseases clinical trials.

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