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  • Register with Our Database

    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: 

    • Studies for healthy males and females 
    • Liver Impairment 
    • Kidney Impairment 
    • Seasonal Allergy

    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.

  • Campus Influencer Program

    Become a Prism Research Campus Influencer and Earn Cash

     Looking for an easy way to earn extra cash this school year?

    Prism Research is recruiting Campus Influencer’s from Colleges and Universities throughout Minnesota.  Interested?  As a Prism Campus Influencer, all you need to do is tell your classmates and friends about upcoming studies and earn $50 for everyone you refer who successfully enrolls in a study. 

    The ideal Campus Influencer candidate:

    •  Is a social media maven. You know how to leverage your Facebook, Instagram, and Twitter networks to work in your favor.

    •  Natural Promoters. You’re always talking about your favorite products and brands.

    •  Willing to promote the Prism Brand on social media and current studies to classmates and friends.

     

    If this sounds like you or someone you know and you’re interested in finding out more about the Prism Research Campus Influencer program, call or email Dayna, 651-724-5047 or daynas@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.

     

     

  • Multiple Sclerosis: Clinical Research Study

    Multiple Sclerosis Study

     

    PRISM CLINICAL RESEARCH 

    Purpose: 

    • To evaluate the safety and tolerability of an investigational drug in individuals with Progressive Forms and/or Relapsing Forms of Multiple Sclerosis.

     

    GENERAL STUDY REQUIREMENTS:   

    • Men and Women, between the ages of 18 and 55.
    • Clinical diagnosis of Primary or Secondary multiple sclerosis or Relapse Remitting or Secondary-Progressive multiple sclerosis.

     

    STUDY DURATION: 

    • 17 Clinic Visits over the course of 76 weeks

     

    METHOD OF ADMINISTRATION:

    • Intravenous Administration

     

    Compensation for Study Participation Time  and Travel

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1812

    Renal Impairment Study

    Clinical RESEARCH study: 1812

     

    PRISM Clinical RESEARCH

     

     

     

     

    Purpose:

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

     

    GENERAL STUDY REQUIREMENTS:

    •  Men and Women Who are not able to become pregnant, between the ages of 18 to 75 with a BMI between 17.5 and 36 kg/m2.
    •  Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION:

    •  In Clinic Stay: 6 nights/7 days.
    •  Clinic Visits: up to 3 including screening and possible Follow-up visit.
    •  Total study duration is approximately 6 weeks (including a 14-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Oral Administration

     

    STUDY COMPENSATION:

    •  Compensation for Study Participation Time Up To: $2,385.00

     

    RECRUITMENT CONTACT:

     

     To prequalify, click here

  • 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 1822

     

    Renal Impairment Study

    Clinical RESEARCH study: 1822

     

    PRISM CLINICAL RESEARCH

     

     

     Purpose:

    •  To assess the pharmacokinetics and to evaluate the safety of an investigational drug in individuals with severe renal impairment versus individuals with normal renal function.

     

    GENERAL STUDY REQUIREMENTS:

    •  Men and Women, between the ages of 18 and 80
    •  Medical conditions and medications must be stable in the opinion of the study doctor.
    •  Volunteers must agree to use contraception, if applicable

     

    STUDY DURATION:

    • In Clinic Stay: 1 in clinic stay of approximately 72 hours, including 24 hours infusion of study drug.
    •  Clinic Visits: 3, including screening visit, visit for PK sample collections and follow up visit.
    •  Total study duration is approximately 38 days (including a 21-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Intravenous

     

    REIMBURSEMENT:

    •  Reimbursement  for reasonable expenses in connection with your Study Participation Up To $1240.

     

    RECRUITMENT CONTACT:

  • Kidney Impairment: Clinical Research Study 1900

    Renal Impairment Study

    Clinical RESEARCH study: 1900

     

    PRISM RESEARCH

     

    Purpose:

    • To evaluate the safety and tolerability of an investigational drug in individuals with type 1 or type 2 diabetes who have been diagnosed with moderate to severe renal impairment.

     

    GENERAL STUDY REQUIREMENTS:

    • Men and women who are 18 years or older with a BMI between 18 and 45
    • Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION:

    • In Clinic Stay: 2 nights/ 3 days
    • Return Clinic Visits: 6 including screening
    • Total study duration is approximately 33 days

     

    METHOD OF ADMINISTRATION:

    • A single subcutaneous injection

     

    STUDY COMPENSATION:

    • Compensation for study participation time up to $1470.00

     

    RECRUITMENT CONTACT:

  • Healthy Males and Females: Study 1901 Cohort 1

    Healthy female and male participants

    Clinical RESEARCH study: 1901 Cohort 1

     

    PRISM RESEARCH

     

    Purpose:

    • To evaluate the safety, tolerability, and pharmacokinetics of an investigational drug being developed for the treatment of certain types of cancer when administered alone and when co-administered with Itraconazole (an FDA approved medication)

     

    GENERAL STUDY REQUIREMENTS:   

    • Men and women who are 18 – 55 with a BMI between 18 to 29.9
    • Must be non-smoker
    • Must be healthy; not being evaluated or treated for any medical conditions unless otherwise approved on a case by case basis by the study doctor

     

    STUDY DURATION: 

    • In Clinic Stay:  2 in clinic stays. The first is 3 nights/4 days and the other is 11 nights/12 days
    • Return Clinic Visits:  4 (including screen)
    • Total study duration is approximately 46 days

     

    METHOD OF ADMINISTRATION:

    • Oral Administration

     

    STUDY COMPENSATION: 

    • Compensation for Study Participation Time Up To: $4184

     

    RECRUITMENT CONTACT:

     

  • Kidney Impairment: Clinical Research Study 1902

    Renal Impairment Study

    Clinical RESEARCH study: 1902

     

    PRISM RESEARCH

     

     

    Purpose: 

    •  To evaluate the safety and tolerability of an investigational drug being developed to ease symptoms of pain and heavy menstrual bleeding associated with endometriosis and uterine fibroids in individuals who have been diagnosed with different levels of kidney impairment compared with individuals with normal kidney function

     

    GENERAL STUDY REQUIREMENTS:   

    •  Women who are 18 years or older with a BMI between 18 to 42
    •  Medical conditions and medications must be stable in the opinion of the study doctor.

     

    STUDY DURATION: 

    •  In Clinic Stay: 6 night/ 7 days (groups 1-4)
    •  In Clinic Stay: 4 night/5 days (group 5)
    •  Return Clinic Visits: 2 including screening
    •  Total study duration is approximately 42 days

     

    METHOD OF ADMINISTRATION:

    •  A single oral dose

     

    STUDY COMPENSATION: 

    •  Compensation for Study Participation Time and Travel Up To: $2170.00 (groups 1-4) and $1570.00 (group 5)

     

    RECRUITMENT CONTACT:

     

  • Liver Impairment: Clinical Research Study 1904

    LIVER IMPAIRMENT: CLINICAL RESEARCH STUDY 1904

    MALES AND FEMALES WITH LIVER IMPAIRMENT

    CLINICAL RESEARCH STUDY: 1904

    PRISM RESEARCH

    PURPOSE:

    • To evaluate the safety, tolerability and pharmacokinetics of an investigational drug in healthy volunteers and volunteers with liver impairment. The investigational drug is being developed for the treatment of impulsive aggression associated with Attention Deficit/Hyperactivity Disorder (ADHD).

    GENERAL STUDY REQUIREMENTS:

    • Men and women between the ages 18-75 years old
    • 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:

    • 1 In-Clinic Stay: Lasting 4 nights/ 5 days
    • Clinic Visits: 1 Screening
    • Total Study Duration is approximately 32 days, including screening

    METHOD OF ADMINISTRATION:

    • Single oral administration

    STUDY COMPENSATION:

    • Compensation for study participation may be provided for time and travel up to $1350

    RECRUITMENT CONTACT:

    Dayna 651-724-5047 or daynas@prismresearchinc.com

  • Seasonal Allergies: Clinical Research Study 1908

    Seasonal Allergy Study

    Clinical RESEARCH study: 1908

     

    PRISM RESEARCH

     

     

     

    Purpose: 

    •  To evaluate the safety and tolerability of an investigational drug in individuals with seasonal allergies.

     

    GENERAL STUDY REQUIREMENTS:   

    •  Men and Women, between the ages of 18-45
    •  Must be healthy and not taking any medications.
    •  Volunteers must agree to use contraception, if applicable
    •  Must have a BMI of 18.5-35kg/m²

     

    STUDY DURATION: 

    •  In Clinic Stay: 3 in clinic stays of 2 nights/ 3 days each.
    •  Return Clinic Visits: 1 screening visit.
    •  Total study duration is approximately 45 (including a 28-day screening period).

     

    METHOD OF ADMINISTRATION:

    •  Intramuscular and nasal spray

     

    STUDY COMPENSATION: 

    •  Compensation for Study Participation Time Up To: $1500.00

     

    RECRUITMENT CONTACT:

     

     

     

  • Healthy Clinical Research Study 1909

    HEALTHY CLINICAL RESEARCH STUDY 1909

    MALES AND FEMALES

     

    PURPOSE:

    •  To evaluate Vitamin D levels in healthy adults

     

    GENERAL REQUIREMENTS:

    • Men and women; 22 years old or older
    • BMI between 18-29.9
    • 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: $75.00

     

    RECRUITMENT CONTACT: Dayna 651-724-5047 or daynas@prismresearchinc.com

     

  • 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 link below:↓

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

Getting to Prism

Prism Clinical Research is located in University Enterprise Laboratories.

1000 Westgate Drive, Suite 149, St. Paul, MN 55114 

When you arrive: 
All outdoor signs read UEL. Parking is Free.
 Enter the main door under UEL awning. 
Turn right as soon as you enter the lobby.
 Prism will be on your right, suite 149.


Prism is conveniently located just two blocks north of the Westgate stop on the Metro Transit Green Line. For complete schedule and route information visit the Metro Transit site.

Click on the map below or see the written directions below to find us.

(Please be advised road construction on HWY 280 will affect your route to Prism)


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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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