Clinical Trial Project Management
Drive success by partnering with an efficient and strategic project management team.
Whether you’re looking to make a mid-study change, configure custom queries, add hardware to your existing eClinical suite, or anything in between — we’ve got you covered.
Global Support
True partnership with a single point-of-contact, plus 24/7/365 support.
Tailored Onboarding
Comprehensive onboarding ensures your clinical trials are confidently up and running in a matter of days to weeks.
Dedicated Expertise
From study timeline reductions to risk mitigation, we expedite your clinical research with ease.
Building a Foundation Together
Our team of dedicated project managers, implementation specialists, data scientists, and product experts are committed to increasing efficiencies and building a strong foundation for compliant clinical trials.
Customer Testimonial
Success Starts with Partnership
Elevate the quality of your trial with a dedicated partner. Whether you’re adding hardware, translating participant-facing study materials, obtaining scale licenses, or anything in between — we’re here to support you.
What Medrio Customers Are Saying
Find out why Medrio has a 98% customer retention rate.
“Built with the builder in mind.”
“One of the easiest systems to implement mid-study updates. Queries are easy to find and respond to. Audit trails are straightforward as well.”
Dan Pontoriero
“The entire team is exceptional.”
“They are reliable and meet timelines. I got the same team members from beginning to end. Working with Ramana was a breath of fresh air!”
Claudia Ramos
SR. DIRECTOR, CLINICAL OPERATIONS
“Data simplified!”
“Medrio provides a system that is versatile and simplifies the complexities of data collection and management for administrators and data managers.”
Anonymous
OUR INTEGRATED SUITE OF SOLUTIONS
Maximize trial efficiency and operational excellence with intuitive clinical data management technology.
Improve data quality, engagement, and retention with a flexible, patient-centric solution.
Efficiently manage informed consent, enhancing compliance and participant experiences.
Drive success by partnering with an effective and strategic project management team.
Proudly Serving Life Science Innovators
Our commitment extends beyond providing solutions; it’s about being a part of a collective effort to drive positive change and innovation in critical sectors of the life science industry.
Frequently Asked Questions
What is clinical trial project management?
Clinical trial project management is a strategic service providing sponsors with a dedicated team of implementation specialists and data experts. We oversee the technical success of your trial, ensuring the Medrio eClinical suite is fully optimized for your specific protocol from setup through closeout.
How do Medrio’s project management services benefit pharmaceutical and biopharmaceutical companies?
We help biopharma companies navigate tight timelines and complex regulatory landscapes. Our project managers specialize in accelerating study startup and ensuring that data management workflows align with the high-stakes requirements of global drug development and GxP standards.
What is the typical onboarding timeline for a new study?
Medrio is recognized for the fastest startup timelines in the industry. Through dedicated project management, most trials can be configured and validated in days or weeks. We focus on rapid eCRF design and database builds to cut industry-average setup times by more than half.
How does the Project Management team handle mid-study changes?
We specialize in managing mid-study amendments with zero downtime. Whether implementing protocol changes or updating study logic, our team provides the technical guidance and support necessary to deploy updates rapidly without interrupting site activities or data collection.
What kind of global support can study teams expect?
Sponsors receive a single point of contact for project management, supported by 24/7/365 global technical assistance. This model ensures that sites worldwide have immediate access to expertise, with a high resolution rate that keeps clinical progress on track across all time zones.
Can Medrio Project Management help fill internal resource gaps?
Yes. Our services act as a “Functional Service Provider” (FSP) model, providing high-level expertise on demand. This allows sponsors to scale quickly for large trials or fill staff vacancies without the long-term overhead of permanent internal hiring.
How does Medrio ensure site and participant materials are ready for global trials?
Our team manages the localization and translation of participant-facing materials, such as eConsent and ePRO forms. We also assist with obtaining necessary scale licenses and configuring hardware to ensure global sites are equipped for high-quality, compliant data collection.
What role does the Project Management team play in risk mitigation?
We conduct expert protocol reviews and provide “sandbox” environments for sponsors to test study builds before going live. By identifying logic conflicts or workflow bottlenecks during the setup phase, we help avoid costly errors and data quality issues later in the trial.
How do these services improve the overall ROI of a clinical trial?
Medrio Project Management drives operational excellence by reducing build times, speeding up database locks, and minimizing manual data reconciliation. These efficiencies lower the total cost of ownership and allow research teams to focus on clinical science rather than technical infrastructure.
Upholding the Highest Compliance Standards
Ready to see Medrio in action? Let’s get started.
