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Physician Partners

Physician
Partners

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

Our concierge-level service begins with our expert staff that is highly trained and experienced in clinical care and research coordinators that are fully certified and vastly experienced in all regulations required for the specialized care with clinical trials. Our staff is backed by an industry-leading compliance and regulatory affairs department that ensures all regulations are adhered to and that we exceed the expectations of our clinical trial partners.

Our staff performs all regulatory submissions, patient recruitment, marketing and business development. At Clinical Endpoints, we partner with physicians who are motivated to provide research as another treatment option to their patients. We are typically the leading enroller of patients globally for the trials we choose to participate in.

Our physician partners typically collaborate with us at one of the three levels below:

Patient
Referral

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)

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)

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.
At Clinical Endpoints our goal is to provide supportive services and education to our physician partners, their patients, and their patient’s families through our dedication to clinical trial excellence. Please email or call us at 480-566-9090 for discussions with our leadership team and other physician partners.

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