Leading Medical Research.
Moving Forward. Together.™
Leading Medical Research.
Moving Forward. Together.™
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At Physicians Research Group, our mission is to improve people's lives through the advancement of safe and effective medical treatments.
Patients / Participants
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Sponsors
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Investigators
We are committed to Investigator Success. We provide study acquisition, document handling, all study related equipment and supplies, and unique marketing materials.
- Participants
- Sponsors
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- Success
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Why Participate?
Patient participants volunteer to assist researcher doctors in testing the safety and efficacy of medications and devices. By participating, you enable countless others to benefit from your efforts.
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Complete an enrollment form for any of our studies or call (800) 774-1534.
Do I Get Paid For Time & Travel?
Most of our research trials will pay you for your time, travel, and/or mileage. We provide payment at each visit or immediately following your visit.
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We consider our your needs and interests first and foremost! You can expect exceptional medical care and unmatched attention to detail from our team of expert physicians and researchers. We will keep you fully informed and completely updated every step of the way.
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Results
We can only be dedicated to sponsor results by remaining 100% Patient-Driven. We have found through our years of successful Clinical Trials and high Industry Success Rates, that when the patient is truly taken care of the numbers take care of themselves.
Large Physician Network
PRG maintains contractual relationships with a large network of specialty physician practices and healthcare institutions for clinical trials
Single Point of Contact
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Our better data is a direct result of an extremely efficient research process coupled with exceptional staff training. The result is patient satisfaction and higher compliance rates which, in turn, leads right back to better data for our sponsors.
Investigators
Top Investigational Partners
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PRG Handles The Daunting Work
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Give Your Patients More
Clinical trials tailored to your practice. With PRG, healthcare providers gain additional treatment options at reduced or no cost and stipends for time and travel.
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An efficient Research Process that is custom tailored to each independent practice and study management services where we handle all the paperwork are just two of the many benefits enjoyed by our Investigators.
Success
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Our expert team of physicians and researchers ensures that all patient data is collected with integrity and accuracy.
Patient-Centric
We conduct research based on patient care, not based on enrollment numbers or demands.
Support
Dedicated research coordinators are assigned to each trial to manage the workload of multiple primary investigators.
Success
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Expansion to sites throughout the United States, Ireland, South America, New Zealand, and Southeast Asia.
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蚂蚁加速器打不开-猴王加速器
1. U.S. Expansion
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2. International Expansion
Difficulty in patient recruitment has led biopharmaceutical companies to shift towards non-US regions for cost efficiency and quick patient recruitment. PRG has offices now in Ireland and New Zealand.
3. Elite Business
PRG has defined roles, expertise, processes, procedures, and profitability. With an established respectable reputation, PRG has secured 100% of healthcare providers approached to participate.
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Amanda Feczko, RN
Director of Regulatory AffairsIntense attention to detail and thoroughness make her a key asset to the PRG team. Specializes in regulatory and FDA compliance as well as implementing and improving quality assurance programs.
Jason Babcock, MBA CMPE
Chief Operating Officer25 years of experience in managing medical institutions with a breadth of healthcare and process knowledge including finance, HR, business development, operational improvement, and customer service.
Emily Babcock, DHS, PA-C
Director of Clinical AffairsDr. Babcock's objective is to enhance relationships between PRG and our principal investigator sites, while educating or re-educating physicians and staff on the current trials and the benefits they pose over the standard of care medications or procedures.
Maureen Banning, RN, FNE
Associate Director of Clinical Affairs & Lead CRC-PRG IndianaTakes novel steps to help provide our principal investigators with additional tools to identify potential patients and truly understand the benefits of clinical trials. Maureen established and runs our Indiana location.
Keri Frye
Clinical Site LiaisonKeri collaborates with our principal investigators, sub-investigators, research staff, and patients to identify new opportunities and resolutions to ensure clinical trial success. She is always available with ongoing, regular communication,