Global site network

We offer end-to-end site management services that enable faster study start-up, efficient site operations, and high patient retention.

At Cavaxion Clinical Research, we deliver comprehensive services across clinical trial operations, site management, and sponsor/CRO partnerships. Our solutions are designed to support both traditional and decentralized models, while prioritizing speed, quality, compliance, and patient-centricity.

We specialize in delivering comprehensive services across clinical trial operations, site management, and seamless collaboration with sponsors and CROs. Whether supporting traditional, hybrid, or fully decentralized clinical trial models, our team is dedicated to upholding the highest standards of speed, quality, compliance, and patient-centricity.

Participants information

What is a Clinical Trial?

Testing the Safety of Medications & Treatments for Future Generations

Clinical trials are research studies where volunteers help scientists find new ways to prevent, detect, or treat diseases. These studies may involve new drugs, combinations of drugs, new delivery methods for existing drugs, or medical devices.

Before a new medication is approved for use, it goes through many tests. First, it’s tested in laboratories, then in animals, and finally in humans. The new medication or device must be proven safe and effective, and often it has to show that it works better than other similar products already on the market.

For Sponsors and CRO's How We Can Assist with Your Clinical Trial?

Clinical Trial Services

Cavaxion partners with sponsors and CROs to support Phase I–IV trials with a full suite of services:

Start-Up Services: Feasibility, PI selection, budgeting, and contracts
Study Coordination: Skilled CRAs and CRCs managing multi-therapeutic trials
Quality Oversight: Real-time source data verification and audit readiness
DCT Support: Remote monitoring, telehealth coordination, eSource, and mobile capabilities
Post-Market Studies: Long-term safety and registry support

How Cavaxion Can Help Principal Investigators Conduct Clinical Trials?

Cavaxion supports Principal Investigators in conducting successful clinical trials through:

Study Design Support: Guidance in creating effective trial protocols.
Patient Recruitment: Advanced systems to streamline participant enrollment.
Site Management: Ensuring smooth operations and regulatory compliance.
Data Management: Maintaining data integrity throughout the trial.
Regulatory Assistance: Navigating approval processes and guidelines.
Budget Management: Optimizing resources and minimizing costs.
Ongoing Support: Training and support for your team.

B2B Sponsor/CRO Support Services

We collaborate with research sponsors, biotech companies, and CROs to streamline study delivery and operational execution.

Custom Solutions Include:

Regulatory Consulting
Guidance on IND, NDA, and regulatory submissions in the U.S. and India.
Trial Design & Feasibility Analysis
Optimizing trial protocols for better patient access and operational feasibility.
Therapeutic Area Expertise
Focused experience in psychiatry, NASH, metabolic disorders, cardiology, vaccine research, and more.
Site Network Access
Connect with our expanding network of trial-ready sites across the U.S., India, and Middle East.
Talent Support
Access our trained CRA/CRC pool for rapid trial staffing needs.