Minimize Risk in Your Oncology Trials: Leverage Our Advanced

Clinical Research Solutions

Accelerate your oncology or Cancer prevention research with Jeeva’s intuitive software to enhance patient engagement, streamline data management, and maximize efficiency.
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We Understand Oncology Clinical Trial Challenges

Patient Recruitment and Retention

Finding and keeping participants in oncology trials is challenging due to the complexity and intensity of treatments. Jeeva’s platform enhances recruitment by reaching a wider patient pool and boosting retention with tailored support and communication tools that keep participants engaged and informed.

Complex Data Management

Oncology trials often involve large, complex datasets. Jeeva simplifies this with centralized data management, allowing researchers to efficiently organize, access, and analyze clinical data, reducing the risk of errors and improving decision-making.

Ensuring Protocol Adherence

Oncology protocols are stringent, and deviations can lead to unreliable data. Jeeva’s software provides automated reminders and an easy-to-use interface to ensure participants and sites adhere strictly to study protocols.

Real-Time Monitoring and Reporting

Timely data analysis is crucial for effective oncology treatments. Jeeva facilitates real-time monitoring and reporting, offering up-to-date insights into patient responses and trial progress for quicker, informed decision-making.

Patient Safety and Compliance

Maintaining high safety standards and ensuring regulatory compliance can be daunting. Jeeva provides built-in compliance features and rigorous data security measures, ensuring adherence to regulatory requirements and prioritizing patient safety.

Communication and Coordination Across Sites

Coordinating between multiple research sites and teams can be cumbersome. Jeeva streamlines communication and data sharing, ensuring all stakeholders have access to the same information, which promotes collaboration and unity throughout the trial.

Patient Journey for Oncology Clinical Research

Rare Disease patient journey

Our Solutions for Oncology Clinical Research

Real-time Centralized Dashboards

Jeeva offers real-time centralized dashboards that streamline the monitoring of oncology trials by providing researchers with instant access to critical data. This feature enables swift assessments and insights, ensuring you’re always informed and can respond promptly to evolving trial dynamics.

Reduce the Logistical Burden

Jeeva's software simplifies managing the logistical complexities of oncology trials. It automates routine tasks, organizes schedules, and minimizes paperwork. This reduction in logistical stress allows research teams to focus more on patient care and study outcomes.

Conduct Research Globally

Expand your oncology research reach by conducting research in 100+ languages to facilitate virtual trials and remote participation. This enables you to effortlessly conduct multi-site research across various regions, providing access to a diverse pool of participants and data.

Premium 24/7 Study Support

We provide premium 24/7 study support, ensuring that your research is continuously monitored and assistance is available whenever needed. Our round-the-clock support helps keep your trial running smoothly, addressing any issues promptly to maintain high study standards.

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Jeeva Benefits

  • Get your study started in less than four weeks
  • 2X faster to first patient first visit (FPFV), half the cost
  • Reduce the logistical burden on study teams by >70%
  • Works on any browser-based device of your choice
  • Real-time centralized monitoring dashboards
  • Premium 24/7 study support
  • Connect with sites and participants from any part of the world

Clients Love Jeeva Solutions 

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Compliance Programs Supported  

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We Hear You Loud and Clear! Clearing Up Your Oncology Research Concerns

You may derive most value when your clinical operations infrastructure is not set up yet. However, even if some of your infrastructure is in place, Jeeva can complement what you have with modularity and automation.

There’s no upfront CapEx. Our pricing is usage-based, and partners see ROI by reducing site coordination and compliance overhead.

That’s exactly why sponsors and CROs with team sizes under 50 people love Jeeva. You get big CRO capabilities without the cost or complexity.

Jeeva is fully validated, GCP-aligned, 21 CFR Part 11 and GDPR compliant. We’re already used by academic medical centers and sponsors in regulated trials.

Jeeva streamlines the recruitment process by leveraging virtual tools to reach a wider audience, helping to connect with diverse patient groups and overcoming geographical barriers to find suitable participants faster.

Jeeva provides centralized dashboards that display real-time data from all active sites, enabling researchers to monitor patient responses, track overall trial progress, and make informed decisions based on up-to-date information.

Absolutely. Jeeva’s robust data management solutions are designed to handle complex and voluminous datasets inherent in oncology trials, making data organization and analysis seamless and efficient.
Jeeva’s platform facilitates global research by supporting virtual trials that allow remote participation and site coordination. This global capability ensures a more comprehensive data collection while providing access to a broader patient pool.
Yes, Jeeva offers premium 24/7 support to ensure that any issues or questions are promptly addressed. This helps maintain consistent study operations and supports researchers at any time, regardless of location.
Jeeva’s software includes built-in compliance features that meet all necessary regulatory guidelines. Automated documentation and security measures are in place to protect data and uphold the highest compliance standards throughout the trial.

Revolutionizing Interventional Radiology: How Jeeva and IR Centers USA are Transforming Patient Outcomes

IR Centers™️ leads Interventional Radiology, offering cutting-edge, minimally invasive treatments in Urology, Gastroenterology, and Orthopedics. With top physician leaders, advanced technology, and nationwide partnerships, they prioritize patient-centric care for exceptional outcomes. As a network partner of Prostate Centers USA®, Hemorrhoid Centers®, and Ortho Centers™️, they are committed to innovation and collaboration in healthcare.

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Still Curious If Jeeva Human-Centric Clinical Research Software Is a Good Fit for Your Study?

Jeeva eClinical cloud is designed to be disease-agnostic, device-agnostic, flexible, and modular to support patient-preferred decentralized or hybrid trial operations. Schedule a 30-minute call today to determine the fit. We will help you identify technology or protocol complexity gaps to enable an informed decision.
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Jeeva Clinical Trials Inc.

10432 Balls Ford Road Suite 300
Manassas, VA 20109
Simplify, Standardize, and Automate Clinical Trials with Human-Centric Software Powered by AI
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