Study Manager

Centralize and Simplify Your Clinical Trials

The Study Manager is your all-in-one powerhouse for managing virtual and site-based clinical trials. With ObvioGo’s intuitive tools, dashboards, and real-time metrics, you can effortlessly streamline consent workflows, compliance monitoring, and participant communication—all while ensuring top-tier data security and regulatory compliance. Designed to centralize and simplify your trial management, the Study Manager empowers your team to capture and securely access data from multiple sources, making it the ultimate solution for efficient and effective clinical trials across any environment.
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Centralized, Secure and Efficient

Managing clinical trials has never been easier. The Study Manager combines the power of Electronic Data Capture with custom workflow management solutions, addressing the unique challenges of remote data collection and participant management. Whether you're monitoring compliance, managing eConsent, or coordinating telehealth appointments, the Study Manager offers a centralized, secure, and efficient platform to streamline your operations.

Enhanced Patient Engagement

Easily manage and monitor participant interactions, ensuring high engagement and compliance throughout the study duration.

User-Friendly Interface

Navigate complex studies with ease using an intuitive, user-friendly interface designed for both novice and experienced users.

Successful Trial Delivery: A Team Sport

In addition to study configuration and management, ObvioHealth partners with leading CROs to optimize and accelerate trial elements. These partnerships allow us to integrate cutting-edge technologies, enhance operational efficiency, and deliver top-tier trial management, ensuring your research is both effective and forward-thinking.

Biostatistics

Our biostatistical support, optimizes study design, creates and tests randomization schemas, and develops statistical analysis plans. These partners also conduct end-of-study statistical analyses and reporting, ensuring thorough and accurate results.

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 collaborates with leading CROs to harness ObvioGo’s automation capabilities and integrations with enterprise clinical research systems, enabling efficient data cleaning, automated edit checks, and advanced query resolution as data is entered, which accelerates the analytical review process.

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Project Management

Our trusted partners provide project management support, taking a proactive and personalized approach to your trial, ensuring smooth execution and success.

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

Our partnered experts handle all aspects of medical writing, from protocols and informed consent documents to peer-reviewed publications, ensuring your study's findings are clearly and accurately communicated throughout the entire 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.

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