Multi-Site Clinical Trial Management and Monitoring
With extensive expertise in a wide range of study types and therapeutic areas, Altasciences’ clinical monitoring and site management teams deliver reliable data, fast. Our experts work closely with you and your sites, to guide you through the complex steps of drug development.
Highly skilled clinical research associates oversee all aspects of your clinical trial conduct to ensure data integrity, patient safety, protocol compliance, and GCP.
Experienced project managers oversee the conduct of multi-site programs in close collaboration with key internal and external stakeholders, ensuring seamless and timely communication.
Whether as stand-alone or part of an integrated program, let’s discuss your clinical monitoring and site management requirements today.
Have 5 minutes? You may be interested in:
- Impaired Renal and Hepatic Function Trials Capabilities
- Full-Time Equivalent Capabilities
- Research Support Services Capabilities
- Integrated Drug Development Services
Altasciences transforms the traditional outsourcing paradigm by simplifying and streamlining drug development solutions, whether for a single study or multiple programs, to offer an integrated/synchronized approach to CRO and CDMO services from lead candidate selection to clinical proof of concept, and beyond.