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Clinical Trial Services

Clinical Trial Services to Meet Your Research Needs

Clinical Trial Services to
Meet Your Research Needs

Clinical Trial Services services offered by GLOBAL include:

•    Clinical Strategy Design
•    IRB/EC/REB Regulatory Submissions
•    Study Plans including Data Management, Monitoring, Safety
•    Trial Master File
•    Site Selection, Qualification, and Initiation
•    Vendor Selection and Management
•    Contract and Budget Negotiations
•    Site Training and Management
•    Data Management


•    Monitoring
•    Trial Branding
•    Investigator Meetings
•    Site Training
•    Case Support
•    Patient Recruitment Strategies
•    Clinical Trial Document Authorship 
•    Publication Authorship and Publication Assistance 
•    Trial Rescue Services

•    SOP Development

Why Choose GLOBAL for Clinical Trial Services?

We work to see through a Sponsor’s vision, while integrating industry best practices and upholding all regulatory requirements. Sponsors maintain ownership and visibility at every step of the process through clear, consistent communication from the clinical team and one of our Project Managers, the single point of contact for study sites on all study related matters. Even though we handle the details, Sponsors will see GLOBAL’s commitment to their vision from start to finish.

Our team collectively has decades of experience in multiple therapeutic areas, including:


•    Cardiac
•    Peripheral vascular
•    Orthopedics
•    Urology
•    Oncology
•    Neurology
•    Dermatology
•    ENT


Our medical device experience spans a broad range of modalities including:

•    IVD
•    Stents (cardiac and PV)
•    Ablation devices
•    ICD/pacemakers and leads
•    Drug coated balloons
•    Bone graft substitutes
•    Drug/device combo products


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