We provide comprehensive services to guide you through the development and execution of a clinical program, across all stages of development and life cycle management.

We have experience and expertise with a diverse range of Therapeutic Areas and focus on innovative, technology enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure your trial is handled with the quality and care that results in compliant outcomes and patient focused results.

Core Services

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Biosafety Services

Sitero handles the committee setup, protocol review, NIH registration, Risk Assessment, IBC charter and will guide the site and investigator through the review and approval process. Sitero handles all amendments and annual reviews.

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Clinical Services

End-to-end clinical research services to help biotechnology, pharmaceutical and medical device companies bring new drugs and devices to the market effectively and efficiently. We have expertise in working with sites and sponsors to break down silos and streamline processes.

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Drug Safety Services

We provide clinical and post-marketing drug safety services, including end-to-end Case Processing, Aggregate Reporting, Clinical Safety Management, Signal Detection, Local PV Representation and audit support.

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IRB Division

Sitero provides independent review committee solutions to ensure participants are protected and research is conducted in a responsible manner across all stages and therapeutic areas. Our services include IRB, IBC, DMC/DSMB and Biosafety consulting services.