Why Tekton?
Where Speed Meets Scientific Passion
At Tekton Research, our mission is to streamline the clinical trial process from start to finish. We excel in rapid study start-up, delivering high quality data, accessing specialized and diverse patient populations, and implementing expert retention strategies that keep participants engaged throughout the research journey.
Your multi-specialty site network for Phase 1-4 clinical trials
Sponsors and CROs partner with Tekton to develop drug, medical device, and diagnostic products across numerous therapeutic areas. Whether you're looking to perform a single-site study or a complex, high-volume trial, Tekton will deliver the right investigators, clinical staff, and patients for your research program.
Neurology & Psychiatry
5+ CNS research sites led by top neurologists and psychiatrists with expertise in Alzheimer's, Parkinson's, Multiple Sclerosis, and more, plus neurology trial capabilities across 10+ general medicine sites
Cardiometabolic
5 endocrinology sites dedicated to cardiometabolic research, plus 10 family physicians who specialize in type 1 and type 2 diabetes, MASH/NASH, obesity, thyroid disorders, and more
General Medicine
20+ leading investigators with proven research experience in obesity, allergies, COPD, asthma, gout, anxiety, depression, atopic dermatitis, osteoarthritis, peripheral neuropathy, and more
Infectious Disease
20+ research sites with proven experience in infectious disease and vaccine research, including flu, RSV, COVID-19, hMPV, combination vaccines, pediatrics, diagnostics, and more
Feasibility and Site Selection
Tekton's feasibility team and investigators deliver precise, timely feedback for optimal site selection. We offer flexible confidentiality arrangements—operating under either a unified agreement or site-specific terms based on your requirements. Our meticulous process ensures you receive a carefully curated list of well-aligned sites with proven experience navigating your specific indication and protocol complexities.
Tekton proposes PIs and sites that are engaged, invested, and dedicated to meeting enrollment goals, providing a positive patient experience, and delivering quality data.
Rapid Start-Up
We understand that time-to-market is critical in clinical research. Tekton Research has streamlined the study initiation process through standardized procedures, dedicated site activation teams, and efficient regulatory submission protocols.
Our clients have a single point of contact who oversees all start-up activities, and can progress from site selection to first patient enrollment in as little as 6-8 weeks. This acceleration doesn't compromise quality—our comprehensive training programs and robust quality assurance processes ensure precision from day one.
Proven Patient Recruitment, Engagement, and Retention Capabilities
Our extensive patient database spans diverse demographic profiles, therapeutic categories, and geographic regions, giving sponsors access to populations that match specific protocol requirements.
Tekton's recruitment strategies combine traditional outreach with digital innovation for precise audience targeting, consistently achieving enrollment targets ahead of schedule.
Our clinical teams and recruitment specialists maintain consistent communication with current participants and our proprietary database contacts, fostering engagement that enhances both future enrollment and current trial retention. By collaboratively involving site staff, providers, and participants in the research process, Tekton prioritizes patient perspectives and needs—delivering an exceptional clinical trial experience.
Advanced Data Management, Quality Assurance, and Regulatory Compliance
All Tekton sites operate under rigorous standard operating procedures (SOPs) and quality assurance initiatives that align with both corporate standards and industry guidelines. Our dedicated Quality Assurance team oversees regular training sessions and systematic updates within our comprehensive quality management system. We conduct routine process reviews to maintain perfect alignment with GCP, ICH, and FDA regulations, ensuring our sites remain audit-ready at all times.
This expertise translates into clean data submissions, minimal queries, and streamlined regulatory interactions, accelerating the path to approval while maintaining the highest ethical standards.