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Global Services
Our Clinical Trials Management Team oversees all types and phases of clinical research, from experimental to observational studies and from early Phase II trials to large multi-center Phase III and Phase IV post marketing studies.

We delegate a project management team uniquely qualified for each project which assures the ongoing compliance with all aspects of clinical procedures and goals.

Through planning, timely implementation and punctual performance of all project responsibilities, combined with time-tested tracking and reporting systems, we possess an impressive track record of completing projects on time, on budget and on target.

Our Clinical Trial Management Services include the following:
  • Clinical Development Plans
  • Phase II, III, IV, Post-Marketing and Safety Surveillance Trials
  • Epidemiological/Market Research Studies
  • Study Protocol, Informed Consent and Case Report Form Design
  • Site/Investigator Identification
  • Pre-study Site Assessment and Selection
  • IRB and Regulatory Authority Approvals and Reporting
  • Preparation of Training Materials/Site Training
  • Site Initiation, Monitoring, and Close-out Activities
  • Clinical and non-Clinical Supplies Logistics and Inventory Development
  • Patient Recruitment Strategies
  • Study Auditing
  • Archiving of Clinical Trial Materials
  • Organization of Investigator Meetings
CONCEPT DEVELOPMENT & STUDY DESIGN
CLINICAL TRIAL MANAGEMENT & SITE MONITORING
CLINICAL DATA MANAGEMENT
BIOSTATISTICS
MEDICAL WRITING & TRANSLATION SERVICES
CLINICAL QUALITY ASSURANCE
MEDICAL AFFAIRS & SAFETY SURVEILLANCE
REGULATORY AFFAIRS
CONSULTANCY & TRAINING SERVICES
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