Clinical Project Administrator en EAST HORN CLINICAL SERVICES IN CEE LIMITED

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Clinical Project Administrator

Fecha de la oferta: 13 Jun.
Empresa que publica esta oferta: EAST HORN CLINICAL SERVICES IN CEE LIMITED
EastHORN Clinical Services in CEE Ltd is a clinical contract research organisation (CRO) serving global pharmaceutical and biotechnology companies in the development of new medicines. The company has operations throughout Central and Eastern Europe. Since starting 12 years ago, we have grown and have established operations in more than 15 countries.

Our international clients value our enthusiastic and flexible approach to meeting their needs and we are growing rapidly.
Número de vacantes: 1
Provincia/s: Madrid

Descripción

Descripción: Main Tasks include, but are not limited to:
 Provides support and coordination in the following functional areas: investigator site
contracts, ethics and regulatory submissions, and review and finalization of essential
documents required for site initiation
 Acts as contact with Regulatory Authorities and Central/Regional Ethics Committees
 Provides clerical support to project team (e.g., word processing, proofreading and
editing correspondence, large and small documents, mailings, shipment of study files,
fax and photocopy documents, assemble study documents, and arrange meetings, etc.)
 Assists in project management activities working with Project Manager or Project
Director (i.e. organizing meetings, taking minutes, following up on outstanding issues
with the study team members; financial data collection and tracking)
 Sets up and maintains clinical investigator files and documentation
 Prepares investigator budget payments and tracking systems; generating tracking
reports as assigned
 Performs data entry and maintenance of selected study tracking databases
 Prepares monitoring visit documentation for Clinical Research Associate
 Prepares study-related documents and other materials for delivery to archives, at
appropriate intervals
 Performs other administrative duties as assigned by management

Requisitos

Requisitos: Competencies

 Excellent written and oral communication skills in Spanish and English
 Excellent organizational and time management skills to handle multiple
priorities
 Ability to work well within a team
 Advanced computer literacy
 Diploma of secondary education or equivalent
 Life science or medical educational background or experience is an advantage
 Experience in clinical trials is an advantage
Nivel de estudios mínimo requerido: BUP / COU / Bachillerato
Experiencia profesional mínima requerida: 1 año
Disponibilidad para viajar requerida: Ninguna

Comparte esta oferta:

Esta oferta ha recibido 86 inscripciones.