The Office of Research Operations oversees the implementation and management of all industry-sponsored, NCI-supported, and grant-funded clinical research across the health system. This office is responsible for operationalizing studies from start-up through closeout to ensure that research is conducted efficiently, compliantly, and with the highest standards of quality. By coordinating study activation, regulatory compliance, participant recruitment, and data integrity, the Office of Research Operations enables investigators to successfully deliver innovative treatment options to patients. Through this work, the office expands access to cutting-edge medical therapies and advances the system’s mission to improve health through research and discovery.
If you represent a pharmaceutical or device company and are interested in FMOL Health as a clinical trial site, please contact us at research@fmolhs.org or (225) 765-7659.
Serving four markets across Louisiana and Mississippi, FMOL Health cares for more than 3 million outpatients and approximately 100,000 inpatients each year.
The racial and ethnic composition of FMOL Health patients is 50.3% white, 28.1% Black, 15.8% unknown and less than 5% other.
The FMOL Health Research Institute offers a streamlined, system-wide research infrastructure designed to deliver high-quality performance for industry-sponsored clinical trials. We provide full-service support to all FMOL Health hospitals, enabling rapid study activation, efficient enrollment, and exceptional regulatory and operational execution.
Our research leadership includes directors of Acute Care and Oncology/Hematology/CAR-T research who oversee a highly skilled team experienced in complex inpatient and outpatient trials. Our study operations workforce features specialized acute care, cardiovascular, oncology, and pediatric research nurses, as well as seasoned clinical research coordinators and research assistants, all trained to meet industry expectations for accuracy, speed, and compliance.
The Office of Sponsored Projects manages all contract and budget negotiations — with dedicated expertise from a grant and contract analyst and a research and grants specialist — ensuring quick turnaround and clear communication for sponsors.
We also maintain a dedicated research regulatory team that handles all IRB submissions and reporting, along with an experienced group of investigational pharmacists who manage and prepare study drugs across the system.
At FMOL Health, we offer sponsors a coordinated, reliable and scalable research environment backed by strong clinical expertise and a commitment to operational excellence.