Sponsors & CROs

The world of clinical research is evolving at an unprecedented pace. Developing new therapies is time-consuming and more costly than ever. Recruiting patients is challenging, and retention can be difficult. Clinical trial participants may not reflect the diversity of the intended use population, even as this becomes an increasingly important priority for sponsors and regulators. Virtual solutions (including telemedicine) may improve access for some, while excluding others. Sponsors are increasingly asking how they can give patients flexibility in their clinical trial experience without compromising data quality.

PCM Trials is your trusted partner to address these challenges. Working in close coordination with sites, pharmacies, laboratories, and other service providers, we serve study participants whenever and wherever is most convenient for them: at home or in long-term care facilities, in the office or at school, even on vacation. This patient-centric approach speeds enrollment, improves retention, enhances adherence, supports diversity and inclusion, and ensures data quality.

PCM Trials directly recruits, trains, certifies, and manages our Certified Mobile Research Nurses (CMRNs) with the commitment that each visit will meet or exceed traditional sites’ standards, both for data quality and patient experience. Our operations support team creates a seamless experience for sites, patients, pharmacies, laboratories, and others involved in each study. We all live Our Values every day as part of our commitment to the many lives we touch: patients, sites, sponsors, and CROs.

Since 2008, we have worked with more than half of the top 20 global biopharmaceutical companies. We have supported clinical studies in the United States, Canada, Europe, Australia, and South America, and we continue to expand our footprint. We combine a global commitment to quality and consistency – including GDPR compliance – with a local awareness of how our CMRNs can best support each research study.

Read About How PCM Trials Supported the TOPAZ Study for People with Parkinson’s Disease

“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.”​
—Sr. Director Clinical Operations, Biopharmaceutical Company
“PCM Trials provided quality service with no deviations, and study study participants were happy to have some study procedures performed in their home.”
—Sr. Project Manager, CRO

Questions? Learn more by downloading our FAQ PDF!

Learn more about how PCM Trials can support your clinical development program
Email: [email protected] or Phone: 888‐628‐9707.