Clinical Research Organization

"You are making me look really good! We couldn’t have done this without Magellan."

VP Clinical Affairs - Stryker Medical

Connecting Knowledge to Needs - Helping You Perform Better


  • Study Design
  • Study Logistics Planning
  • Sponsor Responsibility Oversight / Management
  • Informed Consent Development
  • Risk-based Monitoring
  • Clinical Study Operations
  • Biostatistical Planning
  • Publication Strategy
  • Phase I - IV Studies
  • Post-market Studies
  • Registry Studies


  • Protocol Development / Clinical Investigational Plan (CIP) Development
  • Case Report Form Development
  • Investigator Selection
  • Clinical Trial Agreement Negotiations
  • Site Initiation, Monitoring and Close-out
  • Clinical Study Management
  • Biostatistics / Data Management
  • Clinical Auditing
  • Medical Writing
  • Product Training

Consulting Differently

Your company's future depends on the success of your newest, innovative product. Whether you need regulatory approval, post-market surveillance or to gain critical data to maximize market penetration, this awesome responsibility sits on your shoulders. A thoughtfully conceived, strategically planned and well-orchestrated clinical research trial is not an easy task, especially with limited resources.
Whether you are a team of one or one hundred, Magellan has the clinical research expertise to partner with you on any or all aspects of planning and implementing your study. Or, if you prefer, we can help strategize, develop the protocol and necessary documents, and manage the study for you,from start to finish. We can even assist with operational and oversight responsibilities, if your study is already underway. Our Clinical Research Organization teams aren't just consultants. We're partners, rolling up our sleeves, sitting side-by-side with you and getting the job done.
Get it done now. Get it done right.
Call Magellan today.

Clinical Research Organization Teams

Our Clinical Research Organization teams are comprised of seasoned professionals who have previously worked as:

Clinical Research Directors, Biostatisticians, Research Managers, Clinical Monitors and Analysts, to name a few.

Our Integrated Business Units

  • Marketing and Sales - Product Testing, Voice of the Customer/Patient/Payor, Pricing Sensitivity, Health Economics, Technical Writing, Consensus Summits, Creative Communication, read more
  • Clinical Research Organization - Study Design, Biostatistical Analysis, Phase I - IV, Post-market Studies, Registries, read more
  • FieldSOURCE National Field Teams - Clinical Specialists, Clinical Research Monitors, Sales Associates, Sales Support, Recall Specialists, On-site Specialists, Reimbursement Specialists, read more
  • Reimbursement Solutions - New Code, Appeals, Call Centers, Pre-authorization, Claims Processing, Denials, Improving Revenue Cycle, read more
  • Regulatory and Compliance - FDA and OUS Strategy, Assessment, Compliance, Post-market Support, Quality Systems, read more