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In-house CRA - Multi Sponsor

Laboratory Corporation of America Holdings (Covance)

Budapest, Hungary

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Get ready to redefine what's possible and discover your extraordinary potential at Labcorp Drug Development. Here, you'll have the opportunity to personally advance health-care and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.<br /><br />Join us as we speed the delivery of ground-breaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients-and your career.<br /><br />Labcorp Drug Development is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.</span></p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Role Details:</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">We are looking to recruit an In-House Clinical Research Associate to join our team in Hungary. This is a full time and permanent position. We are open to both experienced and starter-level candidates.</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">As an essential member of the Project Team, the IHCRAs are responsible for supporting the execution of clinical trials. IHCRAs work closely with their CRA colleagues to maintain quality and deliver study milestones in Hungary. </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Responsibilities include but are not limited to:</span></p><ul><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Monitoring site performance and creating action plans for sites not meeting expectations, in conjunction with the site CRA</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Assist CRAs with the preparation for site visits (running reports, QC of files, resolving action items from previous visits)</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Liaise with the project team and others to distribute and track clinical trial supplies to ensure sites have enough to continue recruitment</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Perform Case Report Form review, query generation and resolution, assisting sites as needed</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Document review and collection to ensure compliance and inspection readiness of TMF</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Tracking and processing invoices from investigator sites against agreed contracts and budgets</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: #333740;">Undertake project related administrative tasks (meeting minutes, recruitment tracking, site document preparation)</span></li><li style="margin-bottom: .0001pt;">IHCRA may also be required to attend onsite monitoring visits as a co-monitor with experienced CRAs to assist with tasks such as site regulatory file review and drug accountability</li></ul><h2>Education/Qualifications:</h2><p style="margin: 0px;"> </p><ul><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Research experience in pharmaceutical or CRO industries may be considere</span>d</li></ul><h2>Experience:</h2><ul><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Good organizational and time management skills</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Good communication skills</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Works efficiently and effectively in a matrix environment</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">At least one year of experience in a related field,(i.e.,medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing)</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Fluency in Hungary and English</span></li></ul>

Job posted: 2021-12-21

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