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Study Delivery Services

Ensuring flawless configuration of your study design.

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Bespoke, Tech-Enabled Study Configuration.

Using ObvioGo's code free tools, our in-house delivery team iteratively configures and publishes your trial, sharing insights and working through the 'kinks'  along the way to ensure successful study delivery.

Experienced Teams

Our implementation teams anticipate and mitigate roadblocks to ensure your trial is configured and delivered with digital efficiency and operational excellence.

Internal & External User Testing

We meticulously consolidate internal validation and UAT findings to refine and optimize workflows before launch.

Successful Trial Delivery: A Team Sport

In addition to study configuration, ObvioHealth can offer CRO support to optimize and fast-track trial elements.

Biostatistics

Our in-house biostatisticians can support your trial from the outset to optimize study design, create and test randomization schema and develop statistical analysis plans. They can also conduct end of study statistical analyses and reporting.

Regulatory

Our regulatory experts can serve as your representatives to regulatory authorities, both in the U.S. and abroad. Services include  localization of documentation, operational risk mitigation, and submission management.

Data Management

ObvioHealth data managers can leverage ObvioGo’s  automation capabilities and integrations with enterprise clinical research systems to perform data cleaning, auto edit checks and advanced query resolutions as data is entered, accelerating analytical review.
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Project Management

Our seasoned project managers take a proactive and personalized approach to your trial

Vendor Management

We can oversee vendor qualification, selection, contract negotiation, and training to deliver cost effective results, closely monitoring vendor performance to drive productivity.

Medical Writing

From protocols to informed consent to peer-reviewed publications, our medical writing team can scrupulously translate your study’s findings into clear communications, creating the full scope of clinical trial documentation.

Global Expertise and Client Satisfaction

We are an industry leader, designing and conducting trials across the globe that are optimized to generate more robust and accurate evidence.

89%

Medication Adherence

91%

ePRO Compliance

89%

Retention

2x

Faster Recruitment

40k+

Consented Participants
Average rates for ObvioHealth completed studies (versus industry benchmarks, where applicable)
Designing and delivering trials to a cross-section of industry leaders.