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- Estados Unidos
Hace 21 horas
Al menos 2 años de experiencia, jornada completa, contrato indefinido
To be successful as an Administrative Associate, candidates must possess superior interpersonal, organisational and PC skills (Excel a must and MS Project a plus). At least 2 years of experience in an administrative role. Fluency in host language and English is required.
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.