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  • *NEW INFO* Prism Text

    Prism is excited to announce we have started PRISM TEXT! This texting feature will be a convenient way for the Recruitment Department to TEXT you about upcoming studies. 

    You will be receiving text message from us if you are qualified for a study.

    You are considered OPT-IN unless you tell us to remove you (OPT OUT).

    The texting system is through our secure online database and will not compromise  your phone number. 

     

    Please let us know if you have any questions! 

    Recruitment

    Lindsay 651-368-3360

    Dayna 651-724-5047

    Jenna 651-724-0500

    Andy 651-332-1810

  • Register with Our Database

    Registration form here.

    Get started on the volunteer process by registering your basic information with our database. This information is provided to help us determine your eligibility for current and future studies.

    If you have registered with Prism in the past, please call Dayna 651-724-5047 to update your profile or learn about available studies.

    Find the registration form here

     Unfortunately at this time, Prism can not allow volunteers who live over 200 miles away to participate in research studies. If you live out of state or over 200 miles away please call Geoff at 651-641-2911 with questions. 

    We will not share or sell this info with any third party.

    Thanks for your interest!

  • Upcoming Studies

     

     

     Prism has a variety of upcoming studies to participate in: 

    • Inpatient and Outpatient studies for healthy males and females; Age 18-55 years old
    • Liver Impairment 
    • Kidney Impairment 

    To be put on the call list and receive more information, when available, please contact Dayna at daynas@prismresearchinc.com or Lindsay at lindsayd@prismresearchinc.com.

  • Diagnosed with Liver Impairment?

    Prism Research has upcoming studies for individuals diagnosed with liver impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of liver impairment when compared to volunteers with normal liver function.

     If you or someone you know has been diagnosed with liver impairment and are interested in being considered for these studies, please contact Dayna at 651-724-5047 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

    Please contact Dayna at 651-724-5047 or daynas@prismresearchinc.com

     

  • Diagnosed with Kidney Impairment?

    Prism Research has upcoming studies for individuals diagnosed with kidney impairment.  These studies will help determine how an investigational drug is broken down and removed from the body in volunteers with various degrees of kidney impairment when compared to volunteers with normal kidney function.

     If you or someone you know has been diagnosed with kidney impairment and are interested in being considered for these studies, please contact Lindsay at 651-368-3360 or register with our database and we will call you. Financial compensation for study participation ranges from $400-$3500.

    Please contact Lindsay at 651-368-3360 or lindsayd@prismresearchinc.com

  • Refer Your Friends & Family to Participate

    Simply help us get the word out about Prism Clinical Research and we’ll give you $100 for every friend you refer that completes a study.

    It’s that easy! Make money with each referral, and there’s no limit to how many friends you can refer!

    Rules:

    • Subject must qualify for a study.
    • Subject may not be referred more than one time.
    • Subjects eligible for Referral: (1) Must not be in Prism Clinical Research database; (2) Must not have participated in any prior study at Prism.
    • In the event that a subject is referred by multiple people, the first person who referred will receive payment.
    • Eligibility will be determined by Prism. Prism reserves the right to revise or eliminate this program at any time without notice.

     

     

  • Liver Impairment: Clinical Research Study 1817

    LIVER IMPAIRMENT STUDY

    CLINICAL RESEARCH STUDY: 1817

    PRISM CLINICAL RESEARCH

    PURPOSE:

    • To determine how the investigational drug is absorbed, broken down, and removed from the body in volunteers with abnormal liver function compared to volunteers with normal liver function.

     

    GENERAL STUDY REQUIREMENTS:

    • Men and women between the ages of 18 and 80 years old.
    • Liver Impairment volunteers: must have mild/moderate/severe liver impairment due to diagnosed liver disease.
    • Healthy volunteers: must be healthy; not being evaluated or treated for any medical conditions.

     

    STUDY DURATION:

    • 1 In-Clinic Stay: Lasting 8 nights/ 9 days
    • Clinic Visits: 1(screening)
    • Total Study Duration is Approximately 39 days, including screening

     

    METHOD OF ADMINISTRATION:

    • Oral Administration

     

    STUDY COMPENSATION:

    • Compensation for Study Participation may be provided for time and travel up to $2620.00

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1907

    Renal Impairment Study

    Clinical RESEARCH study: 1907

     

    PRISM RESEARCH

     

    Purpose:

    • To evaluate the safety and tolerability of an investigational drug being developed for  a type of liver disease

     

    GENERAL STUDY REQUIREMENTS:

    • Men and women between the ages of 18-70 with a BMI between 18-38
    • Must be a nonsmoker
    • Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION:

    • In Clinic Stay: 11 nights/12 days
    • Return Clinic Visits: 4 including screening
    • Total study duration is up to 49 days

     

    METHOD OF ADMINISTRATION:

    • Oral Dose

     

    STUDY COMPENSATION:

    • Compensation up to $3980.00for Study Participation Time

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1910

    Renal Impairment Study

    Clinical RESEARCH study: 1910

     

    PRISM CLINICAL RESEARCH 

     

     

     

    Purpose: 

    •  To evaluate the safety and tolerability of an investigational drug in individuals with renal impairment compared to individuals without renal impairment.

     

    GENERAL STUDY REQUIREMENTS:   

    •  Men and Women, between the ages of 18 to 75 with a BMI between 17.5-40kg/m2.
    •  Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION: 

    •  Clinic Visits: 2 (Including screening)
    •  In Clinic Stay: 11 nights/12 days
    •  Follow-Up Visit: via phone
    •  Total study duration may be up to 74 days

     

    METHOD OF ADMINISTRATION:

    •  Oral Administration

     

    STUDY COMPENSATION: 

    •  Compensation for Study Participation Time Up To: $3,885.00

     

    RECRUITMENT CONTACT:

     

     


     [RK1]Please update the version date when the revised version is sent

     [RK2]I believe the draft budget has a total of $3,980. Please confirm which is correct. The ICD also has $3885, so maybe the budget needs to be updated. NOTE: The budget has 2 screening visits included at $95 each.

  • Liver Impairment: Clinical Research Study 1913

    Liver Impairment Study

    Clinical RESEARCH study: 1913

     

    PRISM RESEARCH

     

    Purpose:

    • To evaluate the safety and tolerability of an investigational drug being developed for treatment of certain types of cancer in healthy volunteers and volunteers who have been diagnosed with different levels of liver impairment.

     

    GENERAL STUDY REQUIREMENTS:

    • Men and women between the ages of 18-75 with a BMI between 18-40
    • Liver impairment volunteers: must have mild/moderate/severe liver impairment documented by medical history
    • Healthy Match volunteers: must be healthy; not being evaluated or treated for any medical conditions

     

    STUDY DURATION:

    • In Clinic Stay: 9 days/8 nights
    • Return Clinic Visits: 2 including screening
    • Total study duration is up to 43 (including screening)

     

    METHOD OF ADMINISTRATION:

    • Oral Dose

     

    STUDY COMPENSATION:

    • Compensation for Study Participation Time Up To: $2740.00

     

    RECRUITMENT CONTACT:

  • Sample Trial Available for 70+ year olds: Study 1914

    BLOOD SAMPLE STUDY

    Clinical RESEARCH study: 1914

     

    PRISM RESEARCH

      

    Purpose:

    • To collect blood specimens and clinical data from individuals who have not been diagnosed with heart failure.

     

    GENERAL STUDY REQUIREMENTS:

    • Generally healthy
    • Medication will be approved on a case by case basis

     

    STUDY DURATION:

    • 1 outpatient visit lasting approximately 3 hours

     

    METHOD OF ADMINISTRATION:

    • This is a sample collection study; no study drug will be administered.

     

    STUDY COMPENSATION:

    •  Compensation for Study Participation Time Up To: $85.00

     

    RECRUITMENT CONTACT:

     

  • Connect With Prism Research on Social Media

     

    Have you LIKED Prism Clinical Research on Facebook?

    Have you TAGGED Prism Clinical Research on Twitter?

    Have you FOLLOWED Prism Clinical Research on Instagram?

     

    Use the links below:↓

    https://www.facebook.com/PrismResearch/

    https://twitter.com/ResearchPrism

    https://www.instagram.com/prismclinical_research/?hl=en

     

"I have done studies at different research facilities and Prism is the best

Making the Decision

At Prism Clinical Research, we are committed to a transparent, trusting and open relationship with our volunteers. In fact, we won’t settle for anything less. Because of the nature of clinical research, we depend upon the informed consent of our volunteers – which means our priority is that you understand and are comfortable with our process every step of the way.
And that begins here.


The Volunteer Process

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 Doing the Right Thing

Know that you’ve done your part to help make important medications available to those who need them. If you have a friend or family member who relies on a medication to treat a chronic disease or illness, they have benefited from the work of a clinical trial, and a volunteer like you who gave their time and effort to aid in the approval process. 

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 Fair Compensation for your Time

You’ll be compensated according to your commitment and time spent as a study participant.

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 Medical Exam & Monitoring

As a study participant, you’ll receive a full medical examination and testing for a variety of conditions. In some cases volunteers might have access to treatments or medicines before they are available to the general population.

 

 

Please provide us with your contact information (below) and will get back to you as soon as possible.

If you have a general question, check Volunteer FAQ for an answer. If you're unsure of who to contact, please visit the Contact Us page.

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