Industry Partnerships

At PriMED Clinical Research, we excel in pushing the boundaries of clinical research to foster medical breakthroughs that help change lives. Our dedication to excellence and innovation ensures that every study we undertake contributes meaningfully to the advancement of healthcare.

PriMED Clinical Research collaborates with pharmaceutical and biotechnology firms to explore innovative drugs, medical devices, diagnostics, and combination products. Our commitment to providing timely, high-quality data and exceptional patient care sets us apart in the industry.

Since opening in 2010, PriMED Clinical Research has conducted 85+ trials. Our team of experts has conducted a wide range of clinical indications within family practice and pediatrics.

Feasibility and Patient Access

PriMED offers sponsors rapid and reliable feasibility analysis, supported by our extensive patient network. Our ability to quickly identify qualified patient cohorts is a cornerstone of our research program.

  • Immediate Access to Patients: Our network includes over 60,000 active patients, providing a large and diverse pool for recruitment.
  • Data-Driven Insights: Our dedicated analytics team can query patient data specific to study requirements, ensuring precise and efficient feasibility assessments.

Broad Clinical Expertise

Our investigators and patient population represent a wide range of therapeutic areas, allowing us to support studies across numerous clinical indications.

Our Experience Includes:

Experienced Site Personnel

Our research team is led by two highly qualified Principal Investigators with decades of combined experience, ensuring your study is conducted with the utmost professionalism and clinical expertise.

William Randall, MD
Principal Investigator

  • Board certified in family medicine
  • 15 years of clinical research experience
  • Over 65 clinical trials conducted

Rogelio Amisola, MD
Principal Investigator

  • Board certified in pediatrics and obesity medicine
  • 13 years of clinical research experience
  • Over 25 clinical trials conducted

Additional Staff

Our additional staff aid in managing all study-related activities, including blinded and unblinded roles with available back-ups. This team includes:

  • Two (2) Sub-Investigators
  • Full-time staff of Certified Clinical Research Coordinators (CCRC/CRCs)

Comprehensive Site Capabilities

Our facility is fully equipped to handle the rigorous demands of a wide range of clinical trials. All equipment is professionally maintained and calibrated annually to ensure accuracy and compliance.

  • Diagnostic and Monitoring Equipment: 12-Lead ECG, digital stadiometers, automatic manometers and blood pressure cuffs, and calibrated weight and height measurement devices.
  • Laboratory Capabilities: Ambient and refrigerated centrifuges, with ready access to dry ice for sample transport.
  • Secure Storage: We offer dedicated, climate-controlled, and lockable storage for Investigational Products (IP), along with two 20°C freezers, two 70°C to −80°C freezers, and two 2–8°C research refrigerators.
  • Emergency Preparedness: A fully equipped Crash Cart and AED are on-site to ensure participant safety.

Proven Enrollment Strategies

We understand that timely patient enrollment is critical to study success. Our dedicated recruitment team employs a multi-faceted approach to identify and enroll eligible participants efficiently.

  • Targeted Recruitment: We leverage our ability to query our Electronic Health Record (EHR) system to identify potential candidates, minimizing screen failures and accelerating enrollment.
  • Dedicated Recruitment Team: Our team has extensive experience with external advertisements and community engagement to support recruitment goals.

Efficient Site Activation

PriMED is committed to a rapid and streamlined study start-up process. Our parallel workflows for contract negotiations and IRB submissions are designed to get your study activated quickly.

  • Central IRB: We utilize a central IRB to expedite the review and approval process.
  • Parallel Processing: Contract and budget negotiations occur simultaneously with IRB submissions.
  • Timely Execution: Our team is structured to execute all start-up activities within 30 days.

Partner with PriMED for Clinical Research

Discover the benefits of collaborating with a dedicated and experienced research site. Contact us today to discuss your next clinical trial.

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