Key Clinical Trials - Your partner in clinical research
Become a Clinical Research Site today
Clinical Trials can be a highly valuable asset to both your patients and the practice. Investigative Trials have been vitally important to those suffering from chronic or life-threatening illnesses and can provide patients early access to the latest therapies for a chance at improved medical care. It has also brought medical care to those with inadequate health coverage; all the while generating significant reimbursements for your Private Practice site far above general practice norms.
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(405) 863-2804
About
My responsibility is to the patients in search of novel therapies and new drugs. I will strive to deliver ethical, reliable and first time quality data to our clients. As a well-trained and experienced clinical professional, I remain dedicated to the advancement of clinical treatments for those who need it most.
-Kenny Vo, Owner
Our Services
Key Clinical Trials provides onsite, end-to-end research coordination and daily operations support from study start up to close out. Our responsibilities include study acquisition, patient recruitment, contract/budget negotiations, regulatory maintenance, IRB submissions, data capture and reporting among many others. Leave the heavy lifting to us!
Partnership
Establishing a partnership with us ensures experienced study protocol conduct and precise data collection, compliant with local and federal regulations.
Business Growth
Office-based clinical trials can serve as a significant revenue stream for your practice.
Patient Benefit
Through clinical trials, patients may be often are able to receive treatment at no cost and may be provided with medication they might not otherwise be able to afford.
Frequently Asked Questions
Understanding clinical trials and what it means for you and your practice
Clinical trials are research studies that investigate the safety and efficacy of a new drug or device for the treatment of a medical condition.
Most clinical trial investigators are physicians in private practice. You do not need to be associated with a medical school or a teaching hospital to qualify as a clinical trial investigator. No previous experience as an investigator is needed to qualify.
Clinical trials can significantly boost your bottom line. It’s a great income benefit that comes without having to deal with the hassles of insurers. The biopharmaceutical industry invested more than $15 billion on clinical research at trial sites across the U.S. in 2017. Almost 50% of which went to Investigative Site compensation. Median investigator payment per patient can be $25,000 or more..
Many investigators view participation challenging because of the time and resource commitment necessary. Key Clinical Trials takes on these responsibilities so your regular clinic practice remains undisturbed.
Generally speaking, you have indemnification against actions stemming from a clinical trial as long as you strictly adhere to the protocol and the clinical trial agreement, and you exercise reasonable medical judgment. You should be prepared to provide proof of malpractice insurance to the sponsor or the sponsor’s representative; however, your participation in a clinical trial usually will not impact your premiums.
In a clinical trial, an investigator’s role is to ensure that a study is conducted according to the signed investigator statement, the investigational plan and the applicable regulations. With the help of Key Clinical Trials, these responsibilities, along with many others, are carefully monitored and thoughtfully executed.
As your mutually contracted clinical trials partner, our services come at no cost to you! Contact Key Clinical Trials to learn more.
Clinical trials require a fair amount of management and documentation. Having expert personnel like Key Clinical Trials to handle those components of participation will streamline the incorporation of a clinical trial into your day-to-day practice.
Let us be your Research Partner
Key Clinical Trials seeks to identify and partner with interested clinicians to conduct office-based clinical trials in order to fulfill the emerging needs of the clinical research industry. While assisting pharmaceutical companies and CROs in obtaining their desired targets, Key Clinical Trials provides the necessary site expertise, manpower and training to deliver exemplary research-patient care and high quality data reporting for clinical trials.
Through the highly trained efforts of our dedicated staff and advisors, our team supplies end to end tools to perform study procurement, study feasibility, study start-up, subject recruiting, IRB submissions, contract and budget negotiations, source document and SOP creation, monitoring and auditing preparation, precise data management, regulatory maintenance and many more.
Who will you be working with?
Kenny Vo, Sr. CRA. My experience as a certified Clinical Research Professional with many years of combined Senior Clinical Research Associate (Sr. CRA) monitoring and site level study coordinating offers our partnership a unique edge when it comes to securing and managing studies.
Apart from a credentialed portfolio, my time commitment is my greatest competitive strength, relieving the overwhelming majority of overall physician and site responsibilities.
“I want to make conducting clinical research for you and your practice as simple as possible!” -Kenny Vo, Sr. CRA