At Tranquil Clinical Research, we serve as a trusted Sponsor Oversight partner, providing strategic and hands-on CRO oversight services for pharmaceutical and biotech companies worldwide. Acting as the Sponsor’s oversight arm, Tranquil ensures that outsourced clinical responsibilities are conducted with integrity, compliance, and performance excellence.
We fully integrate with the Sponsor organization and collaborate closely with both Sponsors and CROs to support aligned execution, clear communication, and shared accountability. Our goal is to enhance—not replace—CRO efforts while ensuring Sponsor expectations and regulatory requirements are consistently met.
Tranquil is an industry expert in Site Management, Trip Report Review, GCP and CFR Compliance, Project Metrics, and proactively addressing the study challenges Sponsors often face with traditional CRO models. We are experienced in performing CRO oversight on global levels, managing multiple CROs, overseeing rescue trials, and supporting the execution of emerging pivotal trials.
With a proven history of supporting Global Pharma in CRO oversight roles, Tranquil brings clarity, consistency, and control—ensuring your clinical programs run smoothly from start to finish.