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  India
1) Central Drugs Standard Control
Organization (CDSCO)
2) Indian Council of Medical Research
(ICMR)
3) Department of Biotechnology (DBT)
  International
1) U.S. FDA
2) Center watch
3) International Conference on
Harmonization (ICH)
   
What We Do
  Clinical Trial Design & Management | Clinical Monitoring | Regulatory Affairs | Biostatistics  
  HR Augmentation | Medical and report writing | Auditing and Expert consultation services | Strategic Alliances  
  Additional support services  
 


HR Augmentation Services


Clinical trial management requires enormous resources.

To help manage and meet the resource needs, Arête created a flexible service program that provides  the assistance as per requirements.
All the staff members are fluent in English and regional languages.  We also provide individual staff who can speak local language.
We provide staff in different regions in India.

What We Provide

  • Provide experienced personnel to support  throughout the clinical trial project
  • Helps to manage the resources in an ever-changing industry
  • Ready Back up for any position
  • International standard of service while balancing sensitivity to local needs
  • Regular  development training to all our staff
  • Trained staff working to maintain standards  of the project management

Advantages

  • Provide added value through well trained staff who are committed to their task.
  • Wide range of staff disciplines and experience
  • Excellent staff retention record
  • Help to minimise the costs

Staff required for a clinical trial project

  • Project Managers
  • Clinical Research Associates
  • CTAs
  • Site Coordinators
 
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