Mobile Research Services
Above all, PCM Trials’ mobile research services are flexible: we are committed to patient-centric remote research services that support the full range of sponsor needs. Our Certified Mobile Research Nurses (CMRNs) cover the full range of clinical activities that are within scope for registered nurses and that can be safely delivered with portable equipment. CMRNs travel anytime, anywhere that is convenient for patients, their caregivers, and their families. Patients include pediatrics, the elderly, and every group in between, while therapeutic areas range from rare diseases that affect a few thousand people to the most prevalent indications, such as diabetes and heart disease. We have worked on therapeutics studies from Phase I to Phase IV.
Our CMRNs are backed by an operations support team that is committed to making each patient encounter a success. Project managers work closely with research sites on scheduling, and they coordinate with pharmacies and other suppliers to ensure that each visit has the requisite investigational products and ancillary supplies. Our clinical operations team also supports data integrity and coordinates patient sample logistics. Across our global footprint, data integrity and GDPR compliance are always assured.
- Medication/investigational medical product dosing: infusion, injection, and other routes of administration
- Blood draws, sample collection, and logistics
- Clinical assessment and observation
- Investigational device management
- Patient education and training
- Adverse event monitoring
- Operation of centrifuges, EKGs, and other equipment
- Pharmacy communication and investigational medical product (IMP) coordination
- IMP delivery within stability parameters
- Secure, limited-access, controlled-environment storage
- Mobile visit training
- Inventory management
- Accountability, tracking, and return of unused IP vials/packaging
- Ancillary supply services
- Infusion supplies and pumps
- Syringes
- Lab kits
- Centrifuges
- EKGs
- Sharps containers
- Dry ice
- Coordinate all activities with sites, CMRNs, sponsors, and suppliers
- Confirm visit completion to ensure compliance with protocol
- Quality check source documents for accuracy and completeness
- Ensure strict adherence to clinical trial protocols, good clinical practice (GCP), standard operating procedures (SOPs), and applicable regulations
- Infants
- Pediatrics
- Adolescents
- Adults
- Elderly
- Cardiology
- Cardiovascular
- Dermatology
- Endocrinology
- Gastroenterology
- Genetic Disease
- Gynecology
- Hematology
- Hepatology
- Immunology
- Infectious Diseases
- Musculoskeletal
- Nephrology
- Neurology
- Oncology
- Ophthalmology
- Otolaryngology
- Pediatrics/Neonatology
- Psychiatry/Psychology
- Pulmonary/Respiratory
- Rare Diseases
- Rheumatology
- Transplant
- Urology
- Vaccines
- Virology
- Phase I – Phase IV: dosing and assessment
- Pharmacokinetics/pharmacodynamics
- Real-world data/real-world evidence
- Medical devices
- Natural history
“Having a research nurse come to my house was incredibly convenient. Without this option, I wouldn’t have been able to join the clinical trial. The research nurse who visited my home was very kind and professional. I felt completely at ease.”
– PCM Trials Patient
Learn more about how PCM Trials can support your clinical development program
Email: [email protected] or Phone: 303‐253‐7470.
