Minimize Risk in Oncology Clinical Trials with Connected Clinical Workflows
Support oncology and cancer prevention studies through connected workflows that improve patient engagement, streamline data management, and simplify decentralized and hybrid trial execution.
Problem
We Understand Oncology Clinical Trial Challenges
01
Patient Recruitment and Retention
Recruiting and retaining participants in oncology studies can be difficult due to complex treatment protocols and long study durations. Jeeva helps research teams improve engagement through connected communication and participant workflows.
04
Real-Time Monitoring and Reporting
Research teams need timely visibility into participant progress and study activity. Jeeva supports real-time monitoring and operational reporting across clinical workflows.
02
Complex Data Management
Oncology trials generate large volumes of clinical data across multiple workflows. Jeeva simplifies data coordination through centralized and connected operational visibility.
05
Patient Safety and Compliance
Maintaining safety and regulatory compliance across oncology studies can be operationally demanding. Jeeva supports secure and compliant workflows designed for modern clinical research.
03
Protocol Adherence
Strict oncology protocols require consistent participant and site coordination. Automated reminders and connected workflows help improve protocol adherence across study execution.
06
Communication and Coordination Across Sites
Coordinating across multiple sites and study teams can create operational complexity. Jeeva helps streamline communication and workflow coordination across connected clinical environments.
Problem
We Understand Oncology Clinical Trial Challenges
01
Patient Recruitment and Retention
Recruiting and retaining participants in oncology studies can be difficult due to complex treatment protocols and long study durations. Jeeva helps research teams improve engagement through connected communication and participant workflows.
03
Protocol Adherence
Strict oncology protocols require consistent participant and site coordination. Automated reminders and connected workflows help improve protocol adherence across study execution.
05
Patient Safety and Compliance
Maintaining safety and regulatory compliance across oncology studies can be operationally demanding. Jeeva supports secure and compliant workflows designed for modern clinical research.
02
Complex Data Management
Oncology trials generate large volumes of clinical data across multiple workflows. Jeeva simplifies data coordination through centralized and connected operational visibility.
04
Real-Time Monitoring and Reporting
Research teams need timely visibility into participant progress and study activity. Jeeva supports real-time monitoring and operational reporting across clinical workflows.
06
Communication and Coordination Across Sites
Coordinating across multiple sites and study teams can create operational complexity. Jeeva helps streamline communication and workflow coordination across connected clinical environments.
Problem
We Understand Oncology Clinical Trial Challenges
01
Patient Recruitment and Retention
Recruiting and retaining participants in oncology studies can be difficult due to complex treatment protocols and long study durations. Jeeva helps research teams improve engagement through connected communication and participant workflows.
02
Complex Data Management
Oncology trials generate large volumes of clinical data across multiple workflows. Jeeva simplifies data coordination through centralized and connected operational visibility.
03
Protocol Adherence
Strict oncology protocols require consistent participant and site coordination. Automated reminders and connected workflows help improve protocol adherence across study execution.
04
Real-Time Monitoring and Reporting
Research teams need timely visibility into participant progress and study activity. Jeeva supports real-time monitoring and operational reporting across clinical workflows.
05
Patient Safety and Compliance
Maintaining safety and regulatory compliance across oncology studies can be operationally demanding. Jeeva supports secure and compliant workflows designed for modern clinical research.
06
Communication and Coordination Across Sites
Coordinating across multiple sites and study teams can create operational complexity. Jeeva helps streamline communication and workflow coordination across connected clinical environments.
Solutions
Our Solutions for Oncology Clinical Research
Centralized Real-Time Visibility
Accelerated Recruitment
Access centralized dashboards and connected workflows that support monitoring, reporting, and operational visibility across oncology clinical trials.
Reduced Operational Burden
Flexible & Accessible Participation
Simplify scheduling, coordination, and study workflows to reduce administrative overhead across oncology research operations.
Supported Global Research Participation
Flexible Study Configuration
Enable multilingual participation and decentralized trial workflows across diverse regions, sites, and participant populations.
Premium 24/7 Study Support
Improve Retention & Participant Engagement
Access continuous study support designed to help research teams manage oncology clinical trials efficiently and respond quickly to operational needs.
Jeeva Benefits
Launch oncology clinical trials in less than four weeks
Up to 2X faster to first patient first visit (FPFV) while reducing operational costs
Reduce logistical burden on study teams by over 70%
Access workflows securely across browser-based devices and environments
Real-time centralized monitoring and operational visibility
Premium 24/7 study support for research teams
Connect sites, coordinators, and participants across global clinical trial operations
Clients Love Jeeva Solutions
Compliance Programs Supported
FAQ
We Hear You Loud and Clear! Clearing Up Your Oncology Research Concerns
We already have some of our own tools internally or some third-party vendor contracts.
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.
We’re not ready to invest in new platforms.
There’s no upfront CapEx. Our pricing is usage-based, and partners see ROI by reducing site coordination and compliance overhead.
We’re too small to need something like this.
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.
How do we know it’s compliant?
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.
How does Jeeva’s software facilitate patient recruitment for oncology 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.
What features does Jeeva offer for real-time data monitoring in oncology trials?
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.
Can Jeeva handle the large volumes of data typical in oncology research?
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.
How does Jeeva support global oncology trials?
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.
Is 24/7 study support available through Jeeva’s software?
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.
How does Jeeva ensure regulatory compliance in oncology trials?
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.
We already have some of our own tools internally or some third-party vendor contracts.
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.
We’re not ready to invest in new platforms.
There’s no upfront CapEx. Our pricing is usage-based, and partners see ROI by reducing site coordination and compliance overhead.
We’re too small to need something like this.
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.
How do we know it’s compliant?
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.
How does Jeeva’s software facilitate patient recruitment for oncology 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.
What features does Jeeva offer for real-time data monitoring in oncology trials?
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.
Can Jeeva handle the large volumes of data typical in oncology research?
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.
How does Jeeva support global oncology trials?
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.
Is 24/7 study support available through Jeeva’s software?
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.
How does Jeeva ensure regulatory compliance in oncology trials?
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.
Testimonials
Client Testimonials
In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.
Dr. Emmanuel Gorospe
Chief Medical Officer of KCRS
In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.
Dr. Emmanuel Gorospe
Chief Medical Officer of KCRS
Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.
Marshall Summar, MD, Ph.D
CEO, Uncommon Cures LLC
Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.
Marshall Summar, MD, Ph.D
CEO, Uncommon Cures LLC
We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders
Dr. Terry Jo Bichell
CombinedBrain
We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders
Dr. Terry Jo Bichell
CombinedBrain
Jeeva platform & service is aligned with our vision to making CAR-T cell therapies affordable in emerging markets.
Rahul Purwar
Founder at ImmunoACT
Jeeva platform & service is aligned with our vision to making CAR-T cell therapies affordable in emerging markets.
Rahul Purwar
Founder at ImmunoACT
Jeeva gave us exactly the configurations we needed for our Pivotal clinical trials. I appreciate the functionality of the system.
Mihaela Plesa, BA, CCRP
Director, Clinical Research Programs Frantz Viral Therapeutics
Jeeva gave us exactly the configurations we needed for our Pivotal clinical trials. I appreciate the functionality of the system.
Mihaela Plesa, BA, CCRP
Director, Clinical Research Programs Frantz Viral Therapeutics
In looking for a software partner, our research coordinators and investigators in the field could call the Jeeva team anytime, get reliable support, and have reassurance as we enroll patients on the go. You can count on Jeeva when time is of the essence in operationalizing a clinical trial.
Dr. Emmanuel Gorospe
Chief Medical Officer of KCRS
Jeeva is a game-changer for our rare diseases site/CRO. It is unfair to expect patients or healthy volunteers to visit a hospital or clinic when it is not necessary when a task can be effectively completed safely, remotely, and from the comfort of where they live.
Marshall Summar, MD, Ph.D
CEO, Uncommon Cures LLC
We are pleased to collaborate with Jeeva for the eCOA module for our investigator initiated observational study to understand toileting use by individuals with certain brain disorders
Dr. Terry Jo Bichell
CombinedBrain