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Capabilities


ClinicalRM is a full service CRO that helps clients ensure timely execution of their clinical trials and clinical research projects with highly qualified and experienced teams.  Whether your project is large or small, ClinicalRM can compliment your team or handle your entire trial. Our teams help you navigate and execute clinical trials through FDA approval as an unbiased yet dependable and efficient resource.

Your Project is Our Project

ClinicalRM staff is hired not just for their skills, but also for their team attitude. Our people are flexible, accessible, and adept at stepping into complex situations and becoming part of the team. Our staff is backed by libraries of proven processes, SOPs, work instructions, and templates to have you up and running quickly.

If you have experts on staff, but are missing expertise in key process or tactical areas, or if you have a site but need regulatory advice, monitoring, and data management, our staff is known for being easy to work with and efficient. We check our egos at the door and meld with your team to make the project a success.

If you have a new team, but not enough experience to get a trial to completion, ClinicalRM has a mentoring program that can teach as we go through our trial process.  Finally, if you are missing just a piece of the puzzle, we can provide a single service like monitoring, data management, or drafting submission reports.

Discovery/Pre-Clinical Research
Phase l – lll Clinical Trials
Phase lV Clinical Trials/Post Approval
Staff Augmentation
Regulatory Support

 
 
 
Corporate Headquarters
800.431.9640
330.278.2343


Federal Services Operations
301.620.1987

International Operations
800.431.9640
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