About us​
Learn about our values and approach
At Endpoint Strategy, we specialize in helping MedTech innovators navigate the complexities of clinical trials with confidence. Our boutique consulting model ensures personalized guidance, regulatory clarity, and results-driven execution at every stage.
Our company
We are a team of clinical trial experts with vast experience from the Sponsor, Site, and CRO perspective. From FDA clearance support to end-to-end trial management, we provide tailored strategies designed to streamline development and bring innovative technologies to market faster.

Sharon Branch
Co-Founder
Sharon has 20 years of experience in designing, launching, and executing both pre and post market clinical trials. Her career has uniquely woven together the perspectives of Sponsor, Site, and CRO, giving her a 360-degree understanding of what every stakeholder needs to successfully bring medical technology to patients. She has led complex trials from strategic concept through data lock and submission, built scalable study infrastructure, and nurtured high-performing teams known for excellence in quality and communication.
Sharon co-founded Endpoint LLC to deliver a smarter, more personalized approach to clinical research operations. She specializes in translating clinical strategy into actionable execution, guiding clients through regulatory requirements, site engagement, electronic data capture, day-to-day oversight, and data analysis. Her hands-on experience across the clinical lifecycle fuels her passion for removing friction, anticipating challenges before they arise, and ensuring studies are both inspection-ready and patient-centric.
Sharon co-founded Endpoint LLC to deliver a smarter, more personalized approach to clinical research operations. She specializes in translating clinical strategy into actionable execution, guiding clients through regulatory requirements, site engagement, electronic data capture, day-to-day oversight, and data analysis. Her hands-on experience across the clinical lifecycle fuels her passion for removing friction, anticipating challenges before they arise, and ensuring studies are both inspection-ready and patient-centric.

Michael Conditt, PhD
Co-Founder
Dr. Conditt has 25 years of experience in innovative medical devices, sensors, robotics, biomechanics, and clinical research at medical device startup companies. He has led product management, clinical development, clinical research, and professional education departments at a VP level at multiple small to med size Med Tech companies. Dr. Conditt has authored more than 75 peer-reviewed manuscripts and received numerous academic honors and awards for his research. He earned a PhD degree in biomedical engineering from Northwestern University, where he built a haptic robot to study human motor control, a Master of Science degree in bioengineering from the University of Pennsylvania and a Bachelor of Science degree in mechanical engineering from Texas Tech University.
