CTA Madrid en InVentiv Health Clinical

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Celebramos 25 años


CTA Madrid

Fecha de la oferta: 8 Ago.
Empresa que publica esta oferta: InVentiv Health Clinical
Ver todas sus ofertas de empleo (3)
InVentiv Health Clinical nacida con la vocación de seleccionar los mejores perfiles profesionales del mercado, para ponerlos a disposición del sector farmacéutico. Para inVentiv Health Clinical,cada candidato supone una inversión en concepto de equipo humano, siendo este en todo momento el mayor valor de la compañía y la garantía más segura para el éxito de nuestros clientes.Nacida de la fusión de varias compañía como i3 Pharmaceutical Services y PharmaNet, se convierte en la empresa n 1 del mundo en Outsourcing de personal para investigación clínica
Número de vacantes: 1
Provincia/s: Madrid

Descripción

Descripción: At inVentiv Health, we are currently looking for a CTA to join our organization in Madrid.

Your responsibilities will be:

•Provide (cross functional) clerical and administrative support to project team(s)
•Maintain study-specific tracking reports (e.g. patient enrollment, regulatory documents, site visits)
•Prepare and compile study related materials including investigator meeting binders, training manuals, and Study File Notebooks
•Obtain, review, and process regulatory and administrative documents from investigator sites
•When allocated by study management, collection and preparation of essential/ required documents for submission to a central Institutional Review Board (IRB) or a country's central Ethics Committee, and if necessary based on local requirements the Competent Authority
•Set up, maintain and review regulatory and administrative documents for the Trial Master File (TMF)
•Assist in the identification and recruiting activities for clinical trial investigators
•May (for e.g. training purposes) assist at sites (initially under close supervision from a Clinical Research Associate) to ensure compliance with inVentiv Health Clinical and project SOPs which may require overnight travel up to 50% of the time
•Resolve issues, questions, and requests for additional study supplies
•Review investigator files to ensure all documentation is complete and up-to-date
•Negotiate study budgets with investigators
•Review Case Report Forms (CRFs) and other clinical data for completeness and accuracy
•Resolve queries of CRF data with study site personnel
Edad máxima para el puesto: 65 años.

Requisitos

Requisitos: We are looking for a candidate with the following characteristics:

•High School Diploma or equivalent
•Basic level competence with word processing software (MS Word) and spreadsheet software (MS Excel)
•Good written and verbal communication skills (including English)
•Basic organizational skills
Nivel de estudios mínimo requerido: Licenciado
Idiomas requeridos: Inglés nivel Alto.
Experiencia profesional mínima requerida: 2 años
Disponibilidad para viajar requerida: Ninguna

Comparte esta oferta:

Esta oferta ha recibido 116 inscripciones.