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At Clinical Endpoints, we specialize in providing personalized, concierge-level service to your patients by collaborating with you to offer access to promising clinical trial treatments.

Our concierge service begins with our expert team—certified clinical coordinators with extensive experience in both patient care and regulatory compliance. Our compliance and regulatory affairs department ensures we exceed industry standards and maintain full adherence to all applicable guidelines.

We handle regulatory submissions, patient recruitment, marketing, and business development. Clinical Endpoints partners with motivated physicians to offer research as a treatment option, and we are often a top enroller globally in the studies we support.

Our physician partners typically collaborate with us in one of the three following capacities:

PATIENT REFERRAL

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Many physician practices would like to offer the potential benefits of promising clinical trial treatments to their patients but do not yet have the time or inclination to directly participate in the clinical trial. For such physician practices, we offer a rewarding referral program where we will collaborate with you to provide full clinical trial services to your patients at our office (or potentially yours) through our staff and physicians. And please note that our operations are designed to ensure that there is absolutely no threat of “losing your patients” but rather we help improve your patient services offering and help further build your patient relationships and practice.

SUB-INVESTIGATOR (SUB-I)

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Many physician practices, or individual physicians within a practice, prefer to participate directly in the clinical trial care of their patients. For these physicians, we offer the potential benefits of promising clinical trial treatments to your patients while you provide direct clinical trial-related care. We provide a Principal Investigator (see below), research staff and all compliance and regulatory coverage for the trial in a collaborative environment designed to bring stimulating science, discovery and financial benefit to your practice. We also provide all required Sub-I training in a collaborative and partnership environment.

PRINCIPAL INVESTIGATOR (PI)

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The Principal Investigator carries the highest level of responsibility and risk for participating in a clinical trial. All other trial-related activities are ultimately governed by the PI, including the activities of the Sub-I and all staff. To qualify as a PI, typically physicians begin as a Sub-I and gain significant clinical trial experience. Our PIs all have vast experience and work closely with our expert team to ensure the clinical trial protocol is strictly adhered to and the patient experience is exceptional.

We work with a wide range of industry-leading pharmaceutical sponsors and manage all aspects of study-related activities, allowing you to offer clinical trials to your patients without additional administrative burden.

While we support trials across many therapeutic areas, we specialize in neurology, including:
– Alzheimer’s Disease
– Parkinson’s Disease
– Multiple Sclerosis
– Migraine
– Pain

Our network of providers is always excited to connect with fellow clinicians in the area. We welcome the opportunity to discuss how partnering with Clinical Endpoints can benefit you and your patients.

If you’re interested in learning more, please contact us at info@clinicalendpoints.com.

Clinical Endpoints

9977 N. 95th Street, Suite 101
Scottsdale, AZ 85258
Phone: 480-566-9090
Email: info@clinicalendpoints.com

Operation Times

Monday - Friday
8 am - 5 pm
Evenings and weekends by appointment