PCM TRIALS - Quality Mobile Research Revenue and Competitors

PCM TRIALS is moving the needle on clinical research.\n \nAt PCM TRIALS, our experienced Certified Mobile Research Nurses (CMRNs) bring clinical trial visits to trial participants, wherever they may beâ??at home, work, school, rehab centers, anywhere. Weâ??ve even completed visits in the Alaskan wilderness and backstage at a Broadway show! Plus, weâ??re flexible. So if our clientsâ?? needs change, we adapt with them. The result?\n\n - More participants\n - Better retention\n - Improved protocol compliance and data quality\n - Outstanding results\n\nPCM TRIALS has worked on 180+ protocols for 90+ sponsors and done 20,000+ alternate-site visits.\n \nOur mobile nursing services are available throughout the U.S., Puerto Rico, and with our partners in Canada and overseas. Our management team in Denver, Colorado supports mobile nursing services through project management, quality control and assurance, development of source documents and training, and coordination with CMRNs, participants, sites, labs, pharmacies, etc.\n \nTHE IMPORTANCE OF A CMRN\nAt PCM TRIALS, we donâ??t subcontract research nurses. We employ them. This unique approach results in more control and less risk during trial visits.\n \nEvery PCM TRIALS nurse is trained, tested and certified as a CMRN in the principles of clinical trial research, GCP, Nurse Procedures and Dangerous Goods. Our highly qualified CMRNs travel anytime and anywhere thatâ??s convenient to participants, their caregivers and their families. CMRNs develop positive, trusting relationships with trial participants and provide encouragement during each visit.\n \nOur CMRNs understand the complex and unique requirements of mobile clinical research. Sponsors, CROs and site investigators can be confident that our alternate-site visits are carried out with the same data quality and participant safety as on-site visits across all therapeutic areas.\n \nWHAT SPONSORS ARE SAYING\nThe two biggest challenges in clinical research are recruitment and retention. Dropout rates in clinical trials average about 30%, often because participants get â??visit fatigueâ?? from making multiple trips to investigator sites. Since 2008, the convenience of in-home visits from PCM TRIALS has helped alleviate stress and visit fatigue, increasing retention rates, and trial success significantly.\n \nâ??PCM is highly knowledgeable, flexible and so easy to work with! Their staff members are intelligent, accessible and responsive. I couldnâ??t ask for a better partner in a clinical trial!â??\nâ??Sr. Clinical Manager, CRO\n\n"Thank you to the Clinical Project Manager and Coordinator for always being on top of everything and your quick responses and dedication to our study. We are pleased with PCM TRIALSâ??you are bringing much value to subjects and our study."\nâ??Sr. Director Clinical Operations, Biopharmaceutical Company\n\n"PCM TRIALS provided quality service with no deviations, and study subjects were happy to have some study procedures performed in their home.â??\nâ??Sr. Project Manager, CRO\n\n"PCM TRIALS provides a valuable service where clinical sites are not able to conduct home visits on their own. This service allows for the conduct of protocol where dosing must be observed outside of normal business hours, allowing for an easier site recruitment experience."\nâ??Research Associate, Biopharmaceutical Company