Expediting Phase I to Phase IV projects worldwide on behalf of our clients requires meticulous planning, efficient project management and excellent communication skills to deal with a variety of cultures and local practices.

Chiltern’s Global Clinical Monitoring personnel ensure that the most up to date procedures and strict quality control are adhered to while working with the latest technology. Dedicated local line managers recruit, train and manage clinical monitoring staff to global standards and monitor quality to ICH-GCP, the clinical study protocol, client specific requests and Chiltern Standard Operating Procedures.

Our Global Project Managers are the client’s key liaison focused on global implementation. Working in partnership with clients, investigators and our project teams, the Global Project Managers make the decisions that deliver objectives quickly and efficiently. They perform risk analysis and develop solutions with contingencies for each project as part of our Connect Project Plan. As a result, they share a sense of ownership of the studies and accountability of the project milestones.

Chiltern Global Clinical Development capabilities:

• Global teams located in Americas, Europe, Asia Pacific and South Africa
• Dedicated study teams in key therapeutic areas
• Clinical program development and management
• Project management
• Feasibility research
• Rapid study start up – Chiltern Activate
• Investigator and patient recruitment
• Clinical monitoring
• Safety management
• Site management and training
• Study supply management
• Drug accountability

Chiltern’s emphasis on planning, clear communication and team cooperation across disciplines makes our added value evident from the day a project begins.