At JS Global Hospital, research drives innovation, leading to groundbreaking treatments and life-changing therapies. We actively support physicians participating in clinical trials and research studies, all with the goal of transforming patient care through scientific discovery.
Our clinical studies advance healthcare locally and globally, offering patients access to new and innovative therapies before they become widely available. Participating in clinical research allows patients to contribute to the future of medicine and benefit from the latest medical advancements.
JS Global Hospital operates under a dedicated Institutional Review Board (IRB), responsible for reviewing and approving all research activities. The IRB ensures that all studies meet ethical and regulatory standards to protect patient safety and research integrity.
The IRB team at JS Global Hospital includes expert clinicians and researchers who carefully review proposals, consent forms, and related materials to support responsible, high-quality research initiatives.
We conduct three categories of research, each requiring IRB approval:
Full Board Review
Expedited Research
Exempt Research
Each research project is carefully evaluated to ensure it meets the highest standards of safety, innovation, and ethical responsibility.
JS Global Hospital provides medical students and resident doctors with opportunities to participate in research studies.
This hands-on experience helps future healthcare professionals contribute to scientific discovery and build strong research skills for their medical careers.
At JS Global Hospital, an investigator is any individual involved in conducting human subject research activities. This includes obtaining informed consent, interacting with research participants, and communicating with the Institutional Review Board (IRB).
Investigators are responsible for:
Obtaining information from living individuals through intervention or interaction for research purposes.
Collecting identifiable private information for research.
Securing voluntary informed consent from research subjects.
Studying, interpreting, or analyzing identifiable private information or data for research purposes.
Investigators may include physicians, scientists, nurses, or trained administrative staff. In many studies, one investigator is designated as the Principal Investigator (PI), holding overall responsibility for the study’s conduct.
JS Global Hospital is fully committed to conducting human subject research according to all OHRP and FDA regulations, following ethical standards like the Declaration of Helsinki and the Belmont Report to ensure the highest level of integrity and participant protection.
Our help line is available for study participants, research staff, and team members to share any questions or concerns about clinical research.
Please leave a detailed voicemail — our research team will get back to you within one business day.