Neurology & CNS CRO

Your Easily Scalable, Full-Service CRO

With more than 25 years of expertise in clinical research and data analysis, Omega SMO’s neurology and CNS CRO solutions enable pharmaceutical companies to bring innovative products to market on rapid timelines. We provide localized neurology and CNS CRO services through a global network that assists in trials and post-approval activity across the Americas, Europe, and Asia. This methodology equips us with the resources and delivery centers necessary to quickly coordinate and deploy teams who can consistently work on your project. It’s the way we meet aggressive timelines without compromising quality.

Neurology & CNS Clinical Trial & Research Specialists

With Omega , you get more than just another neurology and CNS CRO. You gain access to industry experts committed to true partnership and collaboration to deliver fast, accurate results. Our experts help accelerate drug and medical device approvals to market by deploying a unique global methodology that enables us to rapidly start projects and fulfill fast timelines.

Omega provides access to more than 1,800 dedicated industry professionals who are committed to your success. Experienced and with outstanding academic credentials, our team is the one you want working on your neurological trials and studies, no matter how large or small. In an industry where turnover is high, we’re proud to have built a company and culture where our people advance, thrive, and stay. Our low turnover rates translate into a more experienced team, consistent quality, and dedicated project management that will support your study’s minute details and big picture from start to finish.

Get a Convenient & Flexible CRO Experience

Our decade-long client partnerships are built on a flexible approach and ease of doing business. Whether for an enterprise-wide global program or single-site study, you’re never stifled by bureaucracy or a rigid, one-size-fits-all model. Our CRO approach is tailored to you and your program: Need to ramp up or down? No problem. Have a last-minute request or change to your trial plan? We’re flexible.

In an industry as fast-moving as ours, we built our business, solutions, and technology to be agile, with your needs at the center. Our deep oncological and data management and analyst experience have earned us a 100% acceptance rate on thousands of CDISC compliant datasets to the FDA and allow us to do the same for you.