Clinical operations

Clinical operations is critical for clinical trial management and works as a guardian for ensuring the reliability of clinical data and subject protection. Symyoo’s Clinical operations team offers solid know-how and experience of study-specific project management, monitoring, and scientific and medical communication for all stages of clinical trials in diverse therapeutic areas. Symyoo’s clinical research associates (CRAs) are highly knowledgeable of good clinical practice and local regulations and are committed to excellence in every study, ensuring the integrity of the study, adherence to protocol, quality of measurements, safety of subjects and valid data.


  • Country Feasibility Assessment
  • Investigator Selection
  • Clinical Trial Agreement Negotiation
  • IRB/EC Approval
  • Site Monitoring Visits
  • Regulatory Document Management
  • Investigational Product Supply Management
  • Scientific and Medical Communication
  • Medical Monitoring
  • Investigator-Sponsored Trial Support
  • Clinical Project Management