Exclusively Trial Management

DSP Clinical Research is a trial management organization headquartered in northern New Jersey. Our focus is to successfully complete your clinical trial while proficiently managing the three key elements to any successful study: investigator site management, study management and site monitoring. We are staffed with project managers with over 15 years of industry experience and regional clinical research associates.

We can set up and manage your Phase I-IV clinical trials from study start up through NDA submission. We can also help you manage multiple vendors such as the central laboratory, central IRB and data management. We also offer customized services such as study rescue, audit of monitors and/or sites and study clean up.

DSP Clinical Research is dedicated to what we do best: managing and monitoring clinical and device trials.

DSP Clinical will always:

• Aggressively meet enrollment timelines
• Aim to get the best services for the best cost
• Stay within budget
• Extensively research therapeutic area and indication
• Provide flexibility and creativity to our clients

Manage Clinical Trials (Phases I - IV)

• Study design
• Document management
• Study set-up and initiation
• Multi vendor management
• On going study and site management
• Monitoring services

• Women's Health
• Endocrinology
• Oncology
• Reproductive Endocrinology
• Central Nervous System
• Cardiovascular
• General Medicine
• Devices

• Web based investigator meetings Interactive voice response systems
• Electronic data capture
• Electronic diaries
• Subject recruitment companies

Contact Information

DSP Clinical Research
Giovanna Kanu, Clinical Project Director
271 Route 46 West, C203
Fairfield, NJ 07004 USA
Phone: 973-797-8803
Fax: 973-276-0707
E-mail:

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