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

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Hi, We Are Happy To Hear From You!

If you would like to learn more about participating in a research study please enter your information and we will get back to you right away!  

Or contact us directly by phone or email!   

Phone | 480-999-5458  

Email | info@doctrials.com  

What Can I Expect If I Participate in a Research Study?

What can I expect if I participate in a research study?

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.

What is a placebo?

A placebo is an inactive, fake, or "dummy" medication or treatment designed to resemble a drug or treatment and given in the same way.  Some studies may include a placebo medication.  This will be outlined in the informed consent document which must be read and signed prior to participation in a clinical study.

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.

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.


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. 



Or enter your information below:

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Studies I am Interested In

Research in Your Practice

DocTrials takes the guess work out of conducting clinical trials in your practice. Clinical trails 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. We provide busy physician practices with everything they need to successfully conduct clinical trials with virtually no disruption to your clinic and no additional overhead.  

What we do:

  • Identify and acquire studies opportunities on your behalf 
  • Provide you with expert Ophthalmic research coordinators who work closely with you conducting patient visits and collecting clean data.
  • Provide you with experienced recruitment coordinators to assist in patient recruitment into studies including: hosting lunch & learns with referral practices, placing advertisements in the community, and conducting chart review in your practice. 
  • Provide you with experienced regulatory coordinators to ensure all institutional review board and federal regulations are explicitly followed. 
  • Provide you with required training including, Good Clinical Practice and Human Subject Protection Training.

Why Should I Participate In Clinical Research?

Professional Development

  • Gain access to cutting edge and novel therapies.
  • Increased opportunity to consult with experts in the field
  • Personal satisfaction knowing you are contributing to the advancement of therapies in your specialty.

Opportunity For Your Practice

  • Increase your patient base through study patient recruitment
  • Gain exposure in the community through study advertising; including radio ads, TV ads, newspaper ads, community outreach, and physician referral outreach. 
  • Increase profits for your practice without adding costly overhead. 




Opportunity For Your Patients

  • Some patients participate in clinical trials because they 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 participate to help others, and improve scientific knowledge.
  • Patients are often reimbursed for their time and travel to study visits. 

"Only about 1 in 8 (13%) physicians currently conduct clinical trials.  Some reasons cited include: no opportunity, too much time required, not enough personnel support, not enough resources, and burdensome paperwork".  Let DocTrials help you overcome these issues and bring research to your practice.

The DocTrials team has made participating in clinical research trials very easy. They are well organized and professional, and they provide access to many interesting projects. Participating in clinical research is rewarding in itself, and it adds a significant new revenue stream that is outside the frustrating world of insurance-based payments.
— Tariq Qamar, MD

For more information about joining our alliance please complete the form below:

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Get in touch

Hi, we're happy to hear from you.  Contact us or complete the form below.

Phone | 480-999-5458

Fax | 480-999-2991 

Email | info@doctrials.com

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Why Use the Physicians in DocTrials?

DocTrials is an alliance of physicians specializing in the conduct of clinical studies.  Sites in the alliance work under core standard operating procedures and quality control measures that provide a methodology ensuring best practice utilization across sites.  This provides assurance and confidence to sponsors that they will achieve quality data in the most efficient and timely manner when placing a study with DocTrials. 

Our Promise:

  • Prompt contract and budget negotiations
  • Prompt completion of regulatory documents
  • Strict adherence to the protocol and all study related procedures and processes
  • Ongoing quality assurance
  • Consistently meet or exceed enrollment expectations
  • Building trust and long term partnerships through constant communication with our sponsors and CROs

I wish all my sites were like yours!
— Tom, Sr. CRA, at a Sponsor
We really enjoyed working with your site on this study and hope to work with you all again on future studies,
— Eric, Project Manager at a Sponsor
I work with DocTrials because I know my studies will be run efficiently from start to finish. Monitors always tell me how much they enjoy working with our team.
— Dr. Mike, Investigator
Your source documents put the sponsor provided source documents to shame!
— Tatiana, CRA at a CRO
It has been a pleasure working with you and your proficient coordinators and regulatory personnel.
— Julie, CRA at a Sponsor
We certainly enjoyed working with your site on the study. Your site is a monitor’s dream.
— Karen, Monitor at a CRO
It was such a pleasure working with you on the *** protocol. Thank you for your dedication and professionalism.
— Judy, a Contract Monitor
It is sites like yours that make my job such a pleasure! :)
— Lindsey, Clinical Ops Manager at a Sponsor

3 Easy Steps to Prepare For Your Visit


1.  Paperwork will be emailed to you to complete and bring to your first visit

2.  Bring questions about the study to discuss with your doctor

3.  Bring a list of your medications and vitamins/ supplements.