With over 30 years of experience

Tranquil Clinical Research provides the expertise you need from study start up to closeout and everything in between.


Protocol, ICF, and CRF Development

Our professionals will ensure your study protocol and study materials are fully GCP-ICH & CFR compliant. Tranquil provides support for all phases (I-IV, post market surveillance, etc).
Learn more

Clinical Trial Management

Tranquil provides support in all aspects of trial management such as protocol development, site selection, budget negotiation, regulatory submissions, study start up, site management, and study closeout.
Learn more

Risk Based Monitoring and Central Monitoring

Tranquil’s approach to identifying trial risks and risk mitigation strategies will ensure your trial is completed with quality and the assurance to appropriately assess study objectives.
Learn more

Monitoring / CRAs

Tranquil provides CRAs with experience in several indications who have been specially trained in adaptive onsite and remote monitoring.
Learn more

Why Tranquil?

Tranquil Clinical Research was created to ensure that the entire clinical trial, device, and drug development process is conducted with ethics and the patient in mind first and always.

The business model ensures a clients drug, device or investigational product in the clinical trial is adherent to the highest level of quality and integrity in the services we provide.

Read More About Us

Find out how our research experts can help with your next study or program.