PRA

Revisa todas las oportunidades que te ofrece PRA. Esta compañía del sector Sanidad te ofrece sus ofertas de trabajo para que encuentres tu próximo empleo.

  • Estados Unidos
  • Sanidad

2 ofertas de empleo

Mostrando 1-2 de 2 ofertas

  • Project Associate

    PRA

    Madrid

    Hace 22 horas

    No se requiere experiencia

    • You will be a recent graduate with an interest in business, project support and the clinical research industry, hoping to secure a role within an award winning company. You will be passionate about making a difference to our business. • To be successful in this role you will be extremely customer focused with a real 'can-do' attitude, have a keen eye for detail and be extremely PC literate (advanced Microsoft Office skills are essential - particularly Microsoft Excel). • We are looking for self-motivated applicants who have exceptional inter-personal skills, and have the ability to learn new tasks and processes quickly in a fast-paced and dynamic environment. You will be tenacious, have high standards of quality with a keen eye for detail and the ability to prioritise and multi task.

  • Clinical Research Associate (CRA)

    PRA

    Zaragoza

    Hace más de 100 días

    No se requiere experiencia, jornada completa, contrato indefinido

    Typical duties for a Clinical Research Associate will likely include preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at site. The Clinical Research Associate (CRA) ensures integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines. Operating as a key part of a global study team, the CRA plays a fundamental role in our clients' drug development processes. The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. Prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential. Fluency in English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. We will positively consider candidates with 33% disability certificate.