Clinical Trials Consultant provide a collaborative approach to the sponsor's needs, with transparent business processes as Medical Affair Manager for Medical device and IMP – from development conduct (MSL/STL or Medical Affair Manager) of Phase I to Postmarket studies to other types of scientific & congress support, medical education and Key Opinion Leader Management (including preparing the KOL for presentations).
Clinical Trials Consultant provide Clinical Project Manager/Clinical trial Lead and Sr CRA for global studies in European Countries (France, Spain, Portugl, Switzerland...) and also Latin America/USA and Canada.
We can provide expert consultancy in the following areas:
Clinical Trials Consultant coordinate feasibility activities including site selection and evaluation, follow up of clinical site management and monitoring activities throughout monitoring visits, drug supply management and review of clinical data with clinical teams and ensuring compliance with regulatory, quality and study requirements.
Clinical Trials Consultant
Calle del Rollo, 10, 1
28005 Madrid SPAIN
Calle Juan Florez 64
15004 A Coruña SPAIN
6, Rue Bonaparte
75006 Paris FRANCE
Teléfono: +34 697485884
Correo electrónico: email@example.com
For publications or to search for a potential investigator’s publication history –
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