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Clinical Research Associate (CRA) / Senior CRA (Монитор клинических исследований)

Медицина и Здравоохранение

    IQVIA (NYSE:Q) is a leading integrated information and technology-enabled healthcare service provider worldwide, dedicated to helping its clients improve their clinical, scientific and commercial results. Formed through the merger of Quintiles and IMS Health, IQVIA's approximately 50,000 employees conduct operations in more than 100 countries. Companies seeking to improve real-world patient outcomes and enhanced clinical trial outsourcing through treatment innovations, care provision and access can leverage IQVIA's broad range of healthcare information, technology and service solutions to drive new insights and approaches. IQVIA provides solutions that span clinical to commercial bringing clients a unique opportunity to realize the full potential of innovations and advance healthcare outcomes.


    Whether you're beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You'll have training and development to plan and progress your career in the direction you choose. And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards. Award winning and innovative, we'll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You'll be building a smart and flexible career with no limits.


    While projects vary, your typical responsibilities might include:

    • Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
    • Supporting the development of a subject recruitment plan
    • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
    • Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
    • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
    • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
    • At least 1 year of independent monitoring experience
    • Alternatively, you should have an equivalent combination of education, training and experience


    You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.


    You should have:

    • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
    • At least 1 year of experience on a position of CRA (or similar) with direct independent on-site monitoring
    • Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
    • Good written and verbal communication skills including good command of English language
    • Good organizational and problem-solving skills


    If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.


    IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.


    We invite you to join IQVIA.