Paid Clinical Trials in Singapore for Healthy Volunteers
Singapore has 7 clinical trials actively recruiting healthy volunteers. These include Phase 1 drug safety studies, bioequivalence trials, vaccine studies, and observational research — most offering financial compensation for participation. Learn which studies pay the most →
Showing 1–7 of 7 studies
A Study of LY3971297 in Healthy Participants
A Study of LY4088044 in Healthy Participants
Improving Vaccine Protection for Adults
A Study of LY4086940 in Healthy Participants and Participants With Overweight or Obesity, With or Without Type 2 Diabetes
A Study of LY4064912 in Healthy Participants and With Overweight or Obesity
Optimizing INtrinsic Capacity for Functional INdependence and to Impede FrailTY in Older Adults: Adaptation of the WHO-ICOPE for Healthy Ageing in Singapore
Hyperpolarized MR Imaging with Carbon-13 Pyruvate in the Human Body
Common questions about trials in Singapore
How many paid clinical trials are recruiting healthy volunteers in Singapore?
There are currently 7 clinical trials actively recruiting healthy volunteers in Singapore. This number updates daily as new studies open and existing studies complete enrollment.
How much do clinical trials pay in Singapore?
Compensation varies by study type and duration. Phase 1 inpatient studies typically pay $1,000–$5,000+, outpatient visits may pay $50–$500 each, and bioequivalence studies often pay $1,000–$5,000. Each study listing includes specific compensation details in the consent form.
What types of healthy volunteer studies are available in Singapore?
Common study types include Phase 1 drug safety trials, bioequivalence studies comparing generic and brand-name drugs, vaccine trials, dietary and nutrition studies, and observational research. All listed studies are registered on public registries and approved by ethics committees.
Do I need health insurance to participate?
No. Healthy volunteer studies cover all study-related medical costs. If an adverse event occurs, the trial sponsor is generally responsible for related treatment. Specifics are outlined in each study's informed consent document.