Why KICS?
With over 100 years of combined experience spanning large and emerging biopharma, our team brings unmatched depth to every engagement. We’ve led clinical trials in oncology, cardiology, infectious diseases, rare diseases, and other therapeutic areas. Today, we channel that broad expertise into helping small and startup biopharma companies succeed. We deliver big-CRO knowledge with the personalized attention of a specialty partner – because your success deserves both scale and heart.
KICS: Your Clinical Research Partner for What’s Next
KICS is a specialized clinical research organization (CRO) built for small biopharma companies. We offer a one-stop shop model that makes high-quality clinical trials accessible, even on modest budgets. Our personalized, white-glove service centers on cost-effective, scalable solutions that bring novel treatments to life without compromise.
Founded to empower emerging biopharma, KICS understands the unique pressures and pace of innovation in early-stage drug development. We’re committed to long-term partnerships grounded in trust, transparency, and shared success.
As a niche CRO, we prioritize collaboration, efficiency, and quality. Our all-women executive team brings deep experience guiding clients through each step of the clinical journey with confidence and clarity.
Let’s collaborate and build something extraordinary together!
KICS was founded to empower small biopharma companies in their efforts to advance medical breakthroughs. As a niche CRO, we focus on efficiency, integrity, and collaboration. Our all-women executive team brings together decades of experience across oncology, rare disease trials, and more, guiding you through every step of the clinical development journey.
We pride ourselves on values of kindness, integrity, commitment, and strength, and are committed to treating your goals as our own. Whether you’re designing a first-in-human study or need a rescue CRO to get a stalled trial back on track, KICS is your agile and reliable partner.
Services Overview
We find the ideal trial sites and investigators tailored to your study’s needs. From patient population considerations to site capability assessments, our team ensures your trial is set up for success at the right locations.
Comprehensive oversight of your clinical study – including study design consultation, regulatory submissions, patient recruitment, and day-to-day project management. We keep your trial on time and in compliance, so you can focus on the science while we handle the operations.
Ongoing support and monitoring for each trial site to ensure protocol adherence, data quality, and regulatory compliance. We build strong relationships with site staff, quickly address issues, and maintain efficient trial conduct from start to finish.
Services Overview
We identify the ideal trial sites and investigators based on your protocol, patient population, and therapeutic area. From feasibility assessments to startup, our team ensures your trial begins with the right partners in the right places.
Our experienced team provides full-service support, including study design consultation, regulatory submissions, patient recruitment strategies, and day-to-day project management. We keep your trial on track and compliant, so you can focus on innovation while we handle the operations.
We offer ongoing oversight to ensure protocol adherence, data quality, and regulatory compliance. By building strong relationships with site staff and proactively addressing challenges, we help ensure efficient, high-quality trial conduct.
WHERE WE'VE WORKED
Discover how KICS can accelerate your clinical journey. Contact us today to learn more about our specialized CRO services and how we can support your next breakthrough.
Choosing KICS means choosing a partner who cares as much about your trial as you do. We measure our success by your success – by studies completed, milestones met, and ultimately, new therapies moving closer to patients. Let’s collaborate to make your clinical development journey efficient, smooth, and successful.