In-house CRA - Multi Sponsor

Πλήρης απασχόληση Γεμάτη μέρα
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.

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.

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.

Vacancy Details:

We are looking to recruit an In-House Clinical Research Associate to join our multi-sponsor team in Greece. This is a full-time, home-based and permanent position.

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 Greece.

  • Monitoring site performance and creating action plans for sites not meeting expectations, in conjunction with the site CRA
  • Assist CRAs with the preparation for site visits (running reports, QC of files, resolving action items from previous visits)
  • Liaise with the project team and others to distribute and track clinical trial supplies to ensure sites have enough to continue recruitment
  • Perform Case Report Form review, query generation and resolution, assisting sites as needed
  • Document review and collection to ensure compliance and inspection readiness of TMF
  • Tracking and processing invoices from investigator sites against agreed contracts and budgets
  • Undertake project related administrative tasks (meeting minutes, recruitment tracking, site document preparation)
  • 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
  • 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)
  • Research experience in pharmaceutical or CRO industries may be considered
  • Good organizational and time management skills
  • Good communication skills
  • Works efficiently and effectively in a matrix environment
  • Experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
  • Fluency in Greek and English
Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant\'s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our

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