Partner with a community-based research site in Central Illinois with direct access to real-world patients, experienced investigators, and a team focused on efficient, high-quality trial execution.
Quality You Trust, Results You Need
Koch Clinical Research helps sponsors accelerate enrollment, improve retention, and deliver high-quality data through a community-based model embedded in primary care.
As a result, sponsors benefit from reliable study execution, consistent communication, and dependable performance across all phases of research.
Sponsor-Focused Execution
Koch Clinical Research supports sponsors and CRO’s through experienced investigators, strong patient relationships, and responsive startup timelines.
As a community-based site embedded within primary care, we provide direct access to real-world patients.
Additionally, our team prioritizes efficient recruitment, clear communication, and dependable trial execution.
Interested in partnering with Koch Clinical Research?
Why Choose Us?
Koch Clinical Research combines experienced investigators, access to real-world patients, and a dedicated research team committed to quality and efficient trial execution.
As a result, sponsors benefit from strong communication, reliable data collection, and consistent study performance.
Site Strengths:
Koch Clinical Research is led by experienced investigators with a proven track record of high-quality clinical trial execution, strong enrollment performance, and exceptional patient retention.
- Experienced Investigators:
Dr. Koch brings 30+ years of clinical research experience across multiple therapeutic areas.
Dr. Imig has 4.5 years as a Principal Investigator with a growing portfolio of successful trials. - Embedded Research Model:
Located within a primary care practice with strong, long-term patient relationships. - Rapid Start-Up Capabilities:
Rapid budget and contract turnaround (typically within 1 business day).
IRB submissions within 1 week of study award. - Proven Enrollment Performance:
Proven enrollment performance across IVD device studies, treatment trials, and healthy volunteer vaccine studies. - Dedicated Research Infrastructure:
Separate research wing with restricted access storage and secure document handling. - Temperature-Controlled Storage:
Refrigerators, freezers (including ultra-low), and drug storage monitored 24/7 with alerts. - Flexible Staffing Model:
Ability to scale quickly using trained clinical staff from the primary care practice. - GCP-Trained Team:
All clinical staff are trained and experienced in GCP for clinical trials.
Where Clinical Research Happens
Koch Clinical Research is committed to delivering reliable, high-quality clinical trial execution through a structured, sponsor-focused approach.
- Efficient feasibility and start-up timelines
- Access to an engaged, real-world patient population
- Consistent communication throughout the study lifecycle
- High-quality data collection and protocol adherence
- A dedicated team focused on reliable study execution
Research Partnerships
Frequently Asked Questions
How can Koch Clinical Research help you find qualified patients for your trial?
We recruit from an established primary care patient population with long-standing provider relationships. As a result, we are able to efficiently identify qualified participants and support strong enrollment timelines. Targeted outreach strategies allow us to expand recruitment when needed.
How do you ensure high compliance and retention during your trials?
We prioritize patient education, clear communication, and consistent follow-up. As a result, our site maintains strong retention and high protocol adherence.
How quickly can your site initiate a new study?
We offer rapid start-up with quick turnaround on feasibility, budgets, and contracts. Typically, IRB submissions are completed within one week of study award.
What makes your site a strong partner for sponsors and CROs?
We combine experienced investigators, a built-in patient population, and a quality-driven team. Additionally, our embedded primary care model supports efficient recruitment and reliable study execution.
