Welcome to Clynergy
/ˈclin-ər-jē/
Noun. The reciprocal action of two or more groups, sources, or other factors to produce an effect that is greater than the effects of each separate source in furthering clinical advancements for the benefit of humanity.
The Clynergy Difference
Clynergy brings more than 19 years of international clinical research experience in all study phases and a wide range of products, including pharmaceuticals, biologics, medical devices, and digital therapeutics. Our services include, but are not limited to, monitoring oversight, risk-based monitoring, risk management, and inspection readiness for sponsor companies and CROs of all sizes. With our expert support, you will save valuable time and resources managing your studies, as well as navigating foreign research environments.
Services
The Clynergy Team is Led by Ned French
Ned's Bio
Ned French is a well-rounded expert in the field of clinical research, with more than 19 years of experience in a variety of roles, including Oversight Risk Manager, Project Manager, Training Manager, Clinical Oversight Lead, Sr. Clinical Research Associate, and Clinical Project Coordinator. He has overseen sites in Phase I facilities, major university hospitals, smaller hospitals, and private practices throughout North America and Europe, working in a broad range of therapeutic areas, including nephrology, central nervous system, hematology, immunology, vaccines, neurology, pain management, wound management, gastroenterology, and surgery.
Mr. French specializes in sponsor oversight; risk management; risk-based monitoring; central and remote monitoring and dashboard development; inspection readiness; project and site management; contracts and budgets; clinical training and CRA development; auditing; medical and technical writing; vendor and partnership management; translation management; systems implementation; and feasibility assessments. In addition to having managed more than 30 in-house studies in support of placebo and product delivery prototype development, he has actively served on over 75 clinical trials, including orphan, biologic, pharmaceutical, and medical device trials.
Having steadily worked his way up through the ranks, in both sponsor companies and clinical research organizations, Mr. French not only understands the “bigger picture,” he also knows first-hand the power of synergistic teamwork in conducting successful clinical trials. What’s more, he has spent the last several years in the international marketplace. Consequently, he is uniquely positioned to design and deliver consulting services that are project-relevant, highly customized, and culturally sensitive.
Mr. French holds a Bachelor of Science degree in Psychology, as well as two high-profile industry certifications – Certified Clinical Research Associate (CCRA) and Certified Clinical Research Professional (CCRP) – which speak to his proven knowledge of the regulations, guidelines, and best practices in the field of clinical research. He is also fluent in English and German.
Experience Counts