Anticipating needs of volunteers and sponsors.

PMG recognizes that to be among the best, our organization must strive to anticipate the needs of our participants and our Sponsors and CRO partners. We are committed to bringing progressive practices and technology to the clinical research process.

PMG offers:

Clinical Team
  • Access to large physician multi-specialty practices and solo practitioners
  • Our team is comprised of Research Coordinators (averaging 5 years experience), Clinical Research Investigators (averaging 10 years experience), administrative, regulatory, recruitment, and laboratory personnel.
  • Site Managers, Network Managers, Directors, and an Executive staff ensure excellence among our sites.
  • Premier staff training and staff retention; web based training capabilities
  • Comprehensive SOPs available through secured electronic access
Patient Recruitment
  • Contractual relationships with large, multi-specialty physician practices and healthcare institutions providing Electronic Health Record (EHR) access to nearly 3 million active patient lives
  • Proprietary database of over 280,000 engaged past or potential research participants
  • Dedicated communications team implements fully-integrated recruitment and retention campaigns including: Physician practice outreach; Community outreach and public relations; Email/direct mail database and external outreach; and Digital, social, and traditional media marketing
Monitoring Area
  • All clinics have customized and dedicated monitoring workspaces
Facility Compliance
  • Secured and climate controlled investigational drug storage
  • CLIA waived laboratories
  • IATA certifications
  • DEA licenses for scheduled drugs
  • OSHA compliant
  • Scheduled equipment inspections and calibration
Standard Equipment and Services
  • Emergency equipment and supplies
  • ECGs
  • Dedicated clinical refrigeration and freezer
  • Remote temperature monitoring via TempGuard
  • Comprehensive diagnostic testing (i.e. radiologic, imaging, and endoscopic procedures)
  • Laboratories equipped for clinical trial specimen processing
  • Lifestyle counseling
  • Ability to use Central IRBs
Information Technology Capabilities
  • Experience with 30 electronic data capture (EDC) systems
  • Fully integrated Clinical Trial Management System (CTMS)
  • Use of Mobile Data Capture System — Clinical Ink™
  • Proprietary software housing the participant database
  • Sponsor portal capabilities
Record Retention Facilities
  • On and off-site storage compliant with U.S. and International requirements
Any Questions?

If you have any questions regarding trial participation, take a moment to read through our Frequently Asked Questions. You may also contact your nearest study center.

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