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CNS Clinical Trial
Management
Clinical Trial
Teams You Can Rely On
At CRC, our team delivers clinical trial management for Central Nervous System (CNS) studies with urgency, precision, and unwavering consistency. From initial planning through data analysis, our experienced project teams drive progress that instills sponsor confidence and keeps trials on track.
More than a service provider, CRC is your CNS CRO partner—anticipating challenges, aligning every detail with your objectives, and executing with excellence. Our approach blends operational rigor with clear communication and scientific insight, ensuring that every milestone moves your program closer to success.
Concierge Support for A Better CRO Experience
CRC will stand by you at every step, offering dedicated project management and rigorous clinical monitoring. From study startup to closeout, CRC’s project leaders are deeply engaged, proactively managing timelines, vendors, and deliverables. Our collaboration transforms the trial experience—instilling confidence that every element is expertly managed.
Through vigilant oversight, seamless communication, and an unrelenting commitment to quality, CRC navigates the complexities of CNS clinical research to deliver actionable data that withstands regulatory scrutiny.
HOW CRC DELIVERS CLINICAL TRIAL MANAGEMENT
01.
CRA Training
Partner with CRC for expertly trained Clinical Research Associates who deliver precise, efficient, and reliable trial monitoring. Our CRAs are trained in CNS-specific assessments and study requirements, ensuring data integrity and consistency across investigative sites.
02.
Document Tracking & Management
Our document management and tracking systems keep your trials organized, compliant, and inspection-ready. With real-time visibility and secure documentation, CRC streamlines study management to ensure accuracy at every touchpoint.
03.
Site Selection, Training & Management
Our team identifies high-performing sites with CNS trial experience, provide specialized training, and maintain ongoing communication to ensure consistency and adherence to protocol—reducing start-up time and improving data quality.
04.
Investigator Selection
CRC carefully matches qualified investigators to each protocol based on indication and experience. Our long-standing relationships with CNS-focused investigators and key opinion leaders accelerate site activation and strengthen study outcomes. Our feasibility process is ongoing, not just a slice in time, as the CNS market constantly changes and the competitive study environment is always changing. Information on our investigators is up-to-date, reliable, and realistic.
05.
Contract Negotiation & Grant Management
Our team of experts negotiate fair, transparent contracts and manage investigator grants efficiently, providing sponsors peace of mind, fiscal control, and on-time payments throughout the study lifecycle.
06.
Planning & Coordination
Our investigator meeting planning and coordination ensure your study launches seamlessly. From logistics to communications, CRC manages every detail so your team stays aligned and focused on study execution.
07.
Comprehensive Vendor Management
CRC’s vendor management spans every critical component—from central labs and ECGs to PET coordination—to maintain quality, reduce risk, and ensure timely delivery. Our teams coordinate vendors with precision, leveraging clear workflows and performance tracking to keep your program on schedule.
CONSISTENCY THAT
DRIVES CONFIDENCE
CRC’s 86% employee retention rate means you will work with the same core team throughout your trial—preserving institutional knowledge, reducing handoff delays, and maintaining momentum. This consistency, combined with our proactive project oversight, allows us to deliver CNS clinical trials that are efficient, compliant, and built to maximize your asset’s chance of success.
get in touch
Ready to partner with a CNS CRO that delivers consistency, clarity, and confidence?
Connect with CRC today to learn how our clinical trial management expertise can accelerate your next program.