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  • Posted: Jul 14, 2022
    Deadline: Not specified
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    PAREXEL has proven to be a trusted partner for the complex development journey required of biopharmaceutical and medical device companies. We’re also an astute guide, able to simplify that journey for our clients, so safe new products can reach patients more quickly. - See more at: https://www.parexel.com/company#sthash.G0bQx8Mi.dpuf


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    Senior Clinical Research Associate (FSP)

    RESPONSIBILITIES

    Parexel FSP is currently seeking Senior Clinical Research Associates & CRAII, home-based, Johannesburg. Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

    Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you. Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

    Some specifics about this advertised role

    • Dedicated to one client.
    • Responsible for all site management and monitoring activities across assigned oncology studies
    • Work with industry leaders and subject matter experts.
    • Opportunity to mentor junior CRAs.
    • Work with world-class technology.
    • Great opportunities to travel, work from home, meet new people and play a pivotal role in the drug development process.

    Here are a few requirements specific to this advertised role.

    • Substantial Site Management experience, with an understanding of clinical trials methodology and terminology.
    • Experience monitoring or willingness to monitor oncology clinical trials.
    • Experience in independent monitoring, all types of visits.
    • Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.
    • Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

    Method of Application

    Interested and qualified? Go to PAREXEL on jobs.parexel.com to apply

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