ClinChoice Clinical Trial Coordination Office: Roles and Features

ClinChoice is a global Contract Research Organization (CRO) that supports the development of pharmaceuticals and medical devices. Their clinical trial coordination office is involved in the following roles and has distinctive features.

Roles

  • Planning and Management of Clinical Trials
    • Support the design, protocol creation, and drafting of clinical trial plans.
    • Manage schedules based on the trial implementation plan to ensure timely progress.
  • Regulatory Compliance and Ethical Review
    • Conduct trial planning and execution in accordance with the regulatory requirements of each country.
    • Coordinate with Institutional Review Boards (IRB/IEC) to ensure ethical conduct of trials.
  • Selection and Management of Trial Sites
    • Select the most suitable trial sites (hospitals, clinics, etc.) and support contract and relationship building.
    • Maintain communication with sites and provide necessary training and support.
  • Patient Recruitment and Informed Consent
    • Develop patient recruitment strategies and support recruitment activities.
    • Assist in obtaining informed consent from participants and provide appropriate information.
  • Data Management and Monitoring
    • Collect, manage, and analyze data to provide high-quality data.
    • Conduct monitoring activities to check the progress of the trial and identify and resolve issues early.
  • Management of Trial Drugs and Supplies
    • Manage the supply, storage, and distribution of trial drugs and related materials.
  • Reporting and Communication
    • Regularly report the progress and results of the trial and maintain close communication with stakeholders.

Features

  • Global Capability
    • ClinChoice has a multinational team providing services that cater to the regulations and cultures of various countries.
    • Utilizing a global network, ClinChoice can conduct trials in a wide range of regions.
  • Advanced Technical Expertise
    • Use state-of-the-art data management systems and analysis tools to ensure efficient and accurate data processing.
    • Implement Electronic Data Capture (EDC) systems to enable real-time data access.
  • Experienced Staff
    • Employ many experts with extensive experience in drug development.
    • Provide support leveraging specialized knowledge in various fields to lead trials to success.
  • Customized Services
    • Flexible response to meet the needs of clients.
    • Assemble dedicated teams for each project to provide detailed support.
  • High-Quality Management
    • Establish a rigorous quality management system to ensure the quality and reliability of trials.
    • Conduct internal and external audits to pursue continuous improvement.

Through these roles and features, ClinChoice’s clinical trial coordination office efficiently and effectively supports clients’ clinical trials, promoting the development of new drugs and treatments.