Cookie Control
Utilizamos cookies para mejorar nuestros servicios y experiencia de usuario. Si continua navegando, consideramos que acepta su uso.

Leer más
Datos para iniciar sesión
¿De qué deseas crear la cuenta?
· Crear cuenta
· Crear cuenta de empresa
· Crear cuenta de sociedad médica

Detalle de la oferta

Datos de empresa

Quintiles and IMS Health have come together to become IQVIA, The Human Data Science Company™ Inspired by the industry we help, IQVIA commits to providing solutions that enable life sciences companies to innovate with confidence, maximize their opportunities and ultimately drive human health outcomes forward.

We provide actionable solutions by tapping into the power of the IQVIA CORE™:

• Domain Expertise.

• Advanced Analytics.

• Unparalleled Data.

• Transformative Technology.

To learn more, visit

Oferta de empleo

Asistente de ensayos clinicos (CTA) con DISCAPACIDAD
Otros Departamentos
Provide administrative support to clinical projects and update clinical systems and databases. Assists with general administrative functions, as required, in support of designated clinical team members.

- Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.

- Collaborate with Clinical Project Manager (CPM), CRAs/iCRAs and RSU on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness.

- Collaborate with CRAs/iCRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

- Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.

- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

- Assist in training and orienting new staff. May act as a mentor for less experienced CTAs.

- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.

- Perform assigned administrative tasks to support team members with clinical trial execution.


Seguro de vida y de salud privado
Ticket restaurant
Horario flexible

Requisitos del candidato

Formación Profesional rama sanitaria
Inglés (Alto)
De 1 a 3 años
- Previous experience in adminsitrative role, ideally as CTA or pharma industry
- Good english level
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint

**Puesto certificado DISCAPACIDAD 30% o superior

Si lo deseas, puedes subscribirte a nuestro boletín de noticias introduciendo tu email a continuación
rss twitter linkedin youtube