About Us

Participating in clinical research is among the most immediate and effective ways to be on the forefront of medical research and discovery. 

 
 

 

 

Patients

Patients who choose to participate in clinical research studies gain access to free doctor visits and often medications with no insurance required. Patients are reimbursed for their time and travel to attend scheduled study visits. Patients receive extra care and testing, they gain knowledge about their condition, and often benefit from the new therapies that are being researched. Patients report deep satisfaction from helping others and contributing to the advancement of scientific knowledge. 

Physicians

Clinical trials with DocTrials are a tested, proven way to grow your practice.  You gain advanced scientific knowledge, specialized expertise, access to new therapies, a broader patient base, and a heightened public profile.  DocTrials connects you with the sponsors, patients, coordination, and support you need to conduct clinical trials, with virtually no disruption to your practice and no additional overhead.  Even the busiest physicians can easily and successfully conduct clinical trials.

SPonsors

Working under core standard operating procedures and quality control our sites provide assurance to sponsors that they will achieve quality data in the most efficient and timely manner.  Our promises includes, prompt and headache-free contract/budget and regulatory completion, meeting or exceeding enrollment expectations, quality data collection, strict adherence to study protocols, long term reliable partnerships - quickening startup and site selections for our sponsor and CRO partners.

Medical advances depend on participation in clinical studies.

 

Participants can gain access to study-related doctor visits and investigational medications at no cost with no insurance required. They may be reimbursed for their time and travel to study visits. They receive study-related care and testing and may gain knowledge about their condition.  

 

 
I have to be honest ... I participated [in a clinical trial] to personally benefit from the trial, but realized that participating can contribute to society as a whole
— Michael

What happens when the study ends?

After a research study is complete, the data collected is analyzed to determine if the treatment are safe and/or of benefit. Often the findings of the study may lead to further research which may include comparing the new drug to commonly used drugs, testing safety and effectiveness in children, etc.  In some cases, the drug or device is approved by the Food and Drug Administration which means that it can be prescribed by a doctor for that disease or disorder.

Where can I learn more about studies?

Visit www.clinicaltrials.gov to learn more about clinical research studies in your area. 

Visit www.nih.gov to learn more about clinical trials and your rights as a participant in a study. 

 

What can I expect?

Prior to participation in a research study your doctor and research coordinator will discuss with you the purpose of the research study and why you would be a good candidate for the study. The required procedures, therapies, potential benefits and possible side effects or discomforts will be discussed.  Once all of your questions have been answered, you will be asked to sign a consent document which outlines specifics of the study.

Will I get paid for my time?

Study participants may be compensated for their time and travel to attend study visits.  In addition, study participants may receive comprehensive labs, EKGs, testing, and investigational medication at no cost.  Medical insurance is not required to participate in a clinical research study.

Should I participate in a study?

People choose to participate in clinical research studies for a number of reasons.  Some participants have been diagnosed with a disease for which no good treatment presently exists.  Some participate to gain access to cutting edge therapy and access to specialists.  Others choose to participate to help others, and improve scientific knowledge.

See what patients have to say about participating in a research study. 

DocTrials gives busy practices everything they need to successfully conduct clinical trials. We identify and acquire study opportunities on your behalf, and provide expert coordinators who work closely with you to implement and administer the research, recruit qualifying participants, and ensure adherence to all institutional review board and federal regulations. 

 

Clinical trials with DocTrials are a tested, proven way to grow your practice. You gain advanced scientific knowledge, specialized expertise, access to new therapies, a broader patient base, and a heightened public profile. DocTrials connects you with the sponsors, patients, coordination, and support you need to conduct clinical trials, with virtually no disruption to your practice and no additional overhead. Even the busiest physicians can easily and successfully conduct clinical trials in their own practices.

 
 

 

Working with a DocTrials site, guarantees the necessary attention to detail on your project.  You will be able to see and feel that Clinical Research is our only business. 

 
 

Strict protocol ADHERENCe

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2 week turn contract/ budget & regulatory

Internal quality assurance

Meet enrollment expectations

 

Weeks to study Start-up/Initiation

Quick start-up timelines attributed to our "Assembly Line" process.
It is sites like yours that make my job such a pleasure! :)
— Lindsey, Clinical Ops Manager, Sponsor
 
“I wish all my sites were like yours!”
— Tom, Sr. CRA, Sponsor

Recent Sponsors & CROs