We are a Site Management Organization focused on enhancing site performance. We conduct phase I-IV clinical trials, giving priority to the efficiency of the patient recruitment process and ensuring an optimal drug development schedule for our clients. Based on our core practices of effective communication, partnership, and flexibility, we develop tailor-made strategies to meet our clients’ specific needs.
We have built up effective, stable relationships with many highly experienced, qualified and active clinical investigators and clinical research coordinators. These include individual practitioners, large single and multi-specialty practices, networks of physicians, hospital-based physicians, and academic medical centers.
All of the investigators in BIOCANCER’s network are evaluated as to their ability to conduct clinical trials, and to ensure that they have the patient populations and administrative capabilities are at their disposal to do so.
It is our philosophy to treat every participant in the clinical trial process with the same degree of respect and consideration. The relationships we have established with investigators and patients are the key to achieving our goal of accelerating the drug development schedule while continuing to ensure the quality of our services.
We have the means to manage clinical development programs from beginning to end, or to work alongside our clients’ staff, enhancing their capabilities. By partnering with BIOCANCER, our clients can be sure that their clinical trial will get the full attention it deserves.
We ensure timely and accurate regulatory board submissions and data collection
All our sites are run by experienced, full-time clinical research coordinators who ensure that regulatory documents are submitted correctly and on time. These teams also account for appropriate site orientation/initiation, patient recruitment, screening and enrollment, as well as the collection of clean and accurate data. Our internal management and quality assurance routines are designed to make sure that every task is performed as quickly and accurately as possible, and that any problem which could jeopardize the trial’s success is identified and resolved.
We provide access to a large patient study population
Prior to contacting an investigator for a trial, we assess the patient population from which the study subjects will be drawn to make sure our enrollment goals can be met. Although we believe that carefully orchestrated advertising can assist in meeting enrollment needs, we firmly believe that the site in question should have its own patient population or internal referral basis from which to enroll patients.
We provide ongoing and effective communication between sites, investigators, and clients
The cornerstones of any successful clinical investigation are mutual support and effective communication. One way we assure this is by appointing a project manager to each study, whose job it is to keep the lines of communication clear and oversee the study from beginning to end. Experience shows that any number of factors can arise during a study that could compromise its outcome. Only professionals with expertise, good problem solving skills and the ability to focus on details can overcome obstacles of this nature. We have the right people for the job.
