Oncology CRO Services

Your Easily Scalable, Full-Service CRO

With a vast pool of expertise in oncological therapeutic research and decades of data management and analysis experience, Omega stands a step above other CROs in providing comprehensive study and trial management in oncology.

Omega overcomes the unique challenges and complexities presented by oncology trials with innovative strategies and technologies for faster, more accurate data capture and analysis. We understand the importance of having a team you can depend on, and our solutions include access to industry professionals with extensive oncology experience. Whether it’s a single-site study or an expansive global research program, we tailor each aspect of our services to the unique needs, scale, and scope of your program.

Oncology Clinical Trial & Research Specialists

With Omega, 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 100 dedicated industry professionals who are committed to your success. Experienced and with outstanding academic credentials, our team is the one you want to work on your oncology 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.

Common Areas of Study Oncological Study

•Hematological Disorders

•Skin Cancer

•Prostate Cancer

•Liver Cancer

•Breast Cancer

•Multiple Myeloma

•GI Cancer

•Lymphoma

•Leukemia

•Lung Cancer

Have a Convenient & Flexible CRO Experience

Our decade-long client partnerships are built on a flexible approach and ease of doing business. Clinical development should not be difficult. 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.