Expertise benefits your clinical trials
Medidata Solutions understands that for technology to provide real business value to your organization, it must be successfully applied to enhance your unique way of performing clinical studies. Our unparalleled global professional services organization can help you get the best value from your investment.
Medidata Professional Services will facilitate and support the complete life cycle of your clinical trial. Industry professionals throughout the world are poised to assist you with your implementation of Medidata products regardless of project size or geography.
Medidata Rave® Implementation Services
Objective: Successful study implementation of your clinical trial
Approach: Planning, consulting, managing and leveraging best practices in study implementation life cycle from study design to study close
Expertise: Project management, study design consulting, study configuration, quality control, data extraction, reporting, integrations and training
Medidata Designer™ Implementation Services
Objective: Improved protocol quality and study start up
Approach: Leveraging best practices in structured and standardized protocol authoring, and facilitating more efficient collaboration and use of protocol knowledge throughout the clinical research process
Expertise: Project management, study design consulting, CDISC and HL7 standards expertise
Medidata Grants Manager™ and CRO Contractor™ Consulting Services
Objective: Effective cost and resource management for your clinical trials
Approach: Planning, consulting, managing and leveraging best practices in investigator and CRO contract management
Expertise: Contract negotiation, research grants, CRO outsourcing and trial resource planning
Benchmarking Consulting Services
Objective: Improved efficiencies and cost savings for your clinical trials
Approach: Analyzing a portfolio of protocols, CRO contracts and investigator grants against comparable industry benchmarks
Expertise: Data analytics, protocol data analysis, contract negotiation, protocol design, research grants, CRO outsourcing and trial resource planning
