Med Clinical Research offers a full range of clinical trial consulting solutions, from project start-up to close-out to meet your clinical trial development needs. We provide experienced clinical research professionals to advance your project goals.
We work very hard to win your trust and keep it. As a team, we strive to understand your goals for every project and set realistic expectations to meet those goals. We do not make promises we cannot keep, We anticipate every risks and complications to ensure we understand your vision. Our centralized-trial support services ensure a quick study start-up to meet enrollment goals, our customized budget pricing ensures we streamline site activation and our preferred research sites ensure all sites in this program are audit-ready.
In the end, our clients see much of themselves in our shared values, and this is why we enjoy working with senior management of small to mid-size pharmaceuticals who are looking for a diverse patient population.
We are an inclusive company, where 60% of our patient pool originates from diverse populations. We also focus on clinical trials and advancing health education of our diverse community.
We take ownership of our work and value each contribution to every project.
We uphold the highest standard of honesty in all that we do.
We value each collaborator and work to achieve the needs of our clients.
Adekunle Adeoti, MD is board certified in internal medicine and gastroenterology. He has over 30 years of clinical experience and 15 years of clinical research experience, serving a culturally diverse population. He is passionate about preventative medicine and GI issues. His area of research include IBS-C, Crohn’s and ciliac disease, mRNA vaccine studies. He is responsible for driving growth in global clinical development where he brings clinical solutions to CRO and biopharmaceutical industries. He brings with him a wealth of global clinical operational and patient enrolment experience across multiple therapeutic experience.
Dr. Dosunmu is a board certified pediatric specialist who is passionate about pediatric and adolescent care. She has been in clinical practice for over 25 years serving a culturally diverse population. She brings a robust pharmacovigilance and protocol development experience to the group. She heads our Pediatric consulting group and has managed clinical development of numerous global pediatric studies.
Tayo is a pharmaceutical research consultant with over 12 years’ of experience in drug and device clinical trial management, Site Management and Project management. She has extensive research career working with pharmaceutical and mid-size CROs clinical trial management in Infectious disease, Cardiac Device, Oncology and Endocrinology therapeutic areas. Her contributions to various projects in early phase and late phase development has brought well known biologics, vaccines and cardiac devices to the market. Tayo has co-authored scientific papers in the Journal of Nuclear Medicine Since starting Med Clinical Research in 2015, Tayo continues to her research career working with small pharmaceutical companies in the monitoring, study management, and drug safety departments. She is an expert at early to late stage drug development with a focus on women’s health and infertility projects. She has extensive experience in scientific evaluation, implementation and execution of Phase I to IV clinical development programs in a variety of therapeutic areas.