Women: Diagnosed with IBS-D? - Payment up to $300. Varies by study. (Chesterfield)

Women: Diagnosed with IBS-D? - Payment up to $300. Varies by study. (Chesterfield)

15 Mar 2024
Michigan, Detroit metro 00000 Detroit metro USA

Women: Diagnosed with IBS-D? - Payment up to $300. Varies by study. (Chesterfield)

Vacancy expired!

Do you or a loved one suffer with irritable bowel syndrome and diarrhea? If so, you may be eligible for research studies in your area.

Research studies are an important part of developing potential future treatment options. Without them, progress in medicine would not be possible. Right now, doctors are looking for people with IBS-D to volunteer for local research studies.

Get Started Now

SEE IF YOU QUALIFY

OR CALL

1-866-551-1907

For more information, visit Research4IBS.com

Those who qualify may receive:

Payment up to $300, which varies by study

No-cost study-related care from local doctors

No-cost study medication

Plus, no health insurance is needed!

About Acurian:

Acurian is a company that recruits people for clinical research studies. We are currently working with pharmaceutical companies to find individuals who are willing to participate in clinical research studies in your area.

In a clinical research study, the participants may receive investigational study product or may receive an inactive substance, or placebo, depending on the study design. Participants receive study-related care from a doctor/research team for the duration of the study. Reasonable payments will be made for participation and the length of the study may vary.

Related jobs

  • Adults with arthritic knee(s) needed for study - $250

  • Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource. EDUCATION/EXPERIENCE REQUIRED : Bachelor\'s degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Two (2) years of relevant experience preferred. Previous coordinator experience preferred. Organizational and analytical and problem solving skills. Demonstrated verbal and written skills at professional level. CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.

Job Details

Jocancy Online Job Portal by jobSearchi.