(XCT669) | Clinical Trial Administrator, Barcelona

(XCT669) | Clinical Trial Administrator, Barcelona

26 dic
|
Importante grupo
|
Barcelona

26 dic

Importante grupo

Barcelona

Job Description:

Description For more than 25 years, Veristat has built a reputation as a thoughtful partner in the clinical development and regulatory submission process. We have done so by hiring talented people who align to our and share a common passion for our mission driven work.Do you value a collaborative work environment and the opportunity to truly make a difference If so, you will feel right at home here. At Veristat, you can grow both personally and professionally, with opportunities to discuss your achievements and advance your career through quarterly feedback conversations and meaningful work.We do things differently than large CROs and would love to have you join our Veristat team! The Clinical Trial Administrator (CTA)

manages Office activities and systems under the supervision of the Directors and supports project teams responsible for conducting clinical studies to agreed timelines on behalf of clients, under the supervision of the Project Manager/Director. As the Clinical Trial Administrator you will:

Create and maintain the Trial Master File documentation Filing of study documentation and providing site support as needed Assist and support company associates in preparation for initiation, monitoring, close down visits and other administrative tasks Develop and oversee tracking systems for study recruitment status, study supplies and other study deliverables Manage delivery of confidential study documentation to all study team members Provide assistance with audits and regulatory inspections Transcribing minutes of meetings Assist with investigator meetings through the preparation, assembly and shipment of training materials Assist with the collection of essential documentation Take telephone calls from team members, investigators and sponsor. Document and follow-up these calls Assist CRA/Project Manager with establishing and implementing the query resolution process Adapt protocols/informed consent forms to country specific requirements Develop/implement project specific monitoring tools and tracking forms under the direction of the Project Manager/Director Welcoming and dealing with guests Managing the Office diary & booking meeting rooms Liaise with external suppliers Maintaining & improving Office systems Monitoring and ordering stationery suppliesExperience & Minimum Requirements:

Computer Literacy including expertise in Importante empresa packages Fluent written and oral English language including familiarity with medical terminology Good oral and written comprehension, professional communication Ability to order and prioritise tasks, self-motivate, and work with minimum supervision Numeracy Good attention to detail Excellent time management skills Good Initiative / Self-starter #LI-remote

El anuncio original lo puedes encontrar en Kit Empleo:
https://www.kitempleo.es/empleo/19889083/xct669-clinical-trial-administrator-barcelona-barcelona/?utm_source=html

Postulate a este anuncio

Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.

Suscribete a esta alerta:
Escribe tu dirección de correo electrónico, te permitirá de estar al tanto de los últimos empleos por: (xct669) | clinical trial administrator, barcelona
Publica un nuevo anuncio gratuito
Necesitas publicar un anuncio? Con más de 1 millón de usuarios únicos al mes en corto encontrarás el candidato ideal para tu empresa, ¿qué estás esperando!
Publica ahora

Suscribete a esta alerta