Clinical Trials Consultant

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). 

  • Conduct thorough feasibility assessments for each of our sponsors’ projects, enabling selection of the most appropriate investigator sites to meet the target of their specific recruitment and study timelines.
  • Our highly experienced in different therapeutic areas (Oncology, CNS, Infectious disease, Cardiology, Medical Devices) clinical research profesional is able to fulfil the most challenging clinical programmes.
  • Clinical Trial Consultant have a clear understanding of clinical research requirements on a global and local country level and have established excellent working relationships with an extensive network of sites internationally (European, US and Latin America).

 

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:

  • Pre-clinical drug discovery and evaluation
  • Clinical study design and protocols for Phase I, II, III and IV studies
  • Regulatory processes in Europe, South Africa, North America and Canada
  • Key message development and branding
  • Marketed product support activities
  • Facilities auditing
  • Project management

 

 

 

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. 



 

Contact

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: info@clinical-trials-consultant.com

 

Clinical Trials Link

For publications or to search for a potential investigator’s publication history –

www.pubmed.org



For information about European oncology centres:

• European Network for Cancer Registries – www.encr.com.fr

For clinical trials information (Clinical Trials NIH) - www.clinicaltrials.gov

For a general guide to internet resources for cancer – www.cancerindex.org

Clinical Trials Consultant will be attending conferences in 2018 and very much hope to meet you there.

Versión para imprimir Versión para imprimir | Mapa del sitio Recomendar esta página Recomendar esta página
© CLinical Trials Consultant

Página web creada con 1&1 IONOS Mi Web.