Mobile Research Services

At PCM Trials, our mobile research services bring clinical trials directly to participants, wherever they are, ensuring that participation is as convenient and comfortable as possible. By prioritizing participant needs, we eliminate geographical and logistical barriers that often prevent involvement in clinical research. Our Certified Mobile Research Nurses (CMRNs) are expertly trained to deliver the full range of clinical activities that are in the scope of registered nurses and can safely be delivered with portable equipment. CMRNs travel anytime, anywhere that is convenient for participants, ensuring high-quality data collection and exceptional patient care.

Mobile visits significantly enhance the inclusivity of clinical trials, allowing diverse populations to participate and receive important medical care without disrupting their daily lives. By bringing trials directly to participants, we speed up enrollment, improve retention rates, and ensure compliance with study protocols, resulting in more efficient and successful studies. Whether at home, work, or even on vacation, PCM Trials is dedicated to making clinical research accessible and seamless for all participants. Watch the video below to learn more about how mobile visits work and how they can benefit your study:

CMRN Services

  • 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

Operations Support

  • 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

Electronic Source Data Capture

At PCM Trials, we ensure the utmost accuracy and security when collecting sensitive health data at home through a secure data management approach within our eSource platform. Our eSource solution streamlines the collection and management of research data by enabling real-time data entry via cellular-enabled tablet devices during mobile visits. This approach:

  • Ensures protocol compliance and data quality
  • Enables anything/anywhere remote monitoring
  • Ensures Principal Investigator oversight and patient safety
  • Complies with 21 CFR part 11, GDPR, and HIPAA
  • Guarantees a comprehensive audit trail

Interested in learning how our eSource solution can improve data collection and security in your study? Watch the video below to learn more about how it works:

Patients

  • Infants
  • Pediatrics
  • Adolescents
  • Adults
  • Elderly

Therapeutic Areas

  • 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

Study Types

  • 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.