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ABOUT US

Pharmaceutical Research Organization, a trial management organization, offers a diverse arena of clinical trial capabilities. We pride ourselves in delivering timely, accurate, and quality results to sponsors and Contract Research Organizations. We insist on producing work of only the highest caliber. Sponsors and CRO’s have the ability to reach our executive officers or any of our trained and research-dedicated clinical study coordinators, 24 hours a day, 7 days a week.

Pharmaceutical Research Organization conducts and manages the day-to-day clinical research trial at the investigative site level on behalf of the Principal Investigator. We handle all correspondence, contracts/budgets, regulatory documents, and training/placement of study-dedicated coordinators at the investigative site to recruit, gather data, document and follow patients. The investigators we work with are not owned by our company, but rather are private practice physicians with large and established practices who contract with us on a protocol-to-protocol basis to assist them in conducting the trial at their practice site. It is a symbiotic relationship that has worked extremely well for all parties.

Pharmaceutical Research Organization conducts mainly Phase II-IV clinical research protocols. Since February 2000 we have worked with over 45 Principal Investigators at 29 sites, conducted 350 protocols and enrolled over 10,000 patients.

Pharmaceutical Research Organization works hand-in-hand with the study Sponsor and their representatives, Institutional Review Boards, Investigative Sites and patients to facilitate a smooth clinical trial process from onset to completion by:

  • Identifying Qualified and Experienced Investigative Sites
  • Protocol Review and Feasibility Analysis for Investigative Sites
  • Recruitment and Training of a Principal Investigator, and any Sub-Investigators
  • Recruitment and Training of Ancillary Clinical Staff as appropriate
  • Contract and Budget Negotiation
  • Regulatory Affairs Management
  • Research-Dedicated Study Coordinator
  • Placement and Training
  • Patient Recruitment and Screening
  • Qualified Patient Enrollment and Follow-Up
  • Data Collection
  • Internal Quality Assurance
  • GCP/ICH Annual Training for Principal Investigators
  • Continuing Education