SCIRENT is a specialized contract research organization (CRO) focused on cardiovascular advancements. We enable cutting-edge research tailored to the needs of biotech and medtech clients. Our expertise drives innovations that shape the future of patient care and medical research.
SCIRENT offers the Study Nurses Program to overcome geographical and logistical challenges in healthcare. This initiative ensures patients have access to specialized cardiovascular care and clinical trials, no matter their location. SCIRENT’s Study Nurses serve as a vital link between patients in remote areas and cutting-edge cardiovascular medicine. These highly skilled professionals provide expert, compassionate care and play a key role in advancing SCIRENT’s research efforts.
SCIRENT offers the Field Engineers Initiative to support the use of medical devices in clinical studies. These technical experts ensure seamless research execution and uphold the highest standards of data integrity and reliability. Field engineers play a critical role in advancing new therapies and technologies by maintaining accuracy in every piece of collected data. Their meticulous work drives SCIRENT’s contribution to groundbreaking discoveries and innovative treatments in cardiovascular care.
Long-standing relationships with the sites give our team direct access to study staff
Our Flying Nurses and Field Engineers deliver expert cardiovascular care and technical support.
Our site coordinators play a crucial role in the execution and management of clinical trials at specific research sites. They ensure that the site is prepared for the trial, including setting up necessary infrastructure, training staff, and ensuring that all regulatory and compliance requirements are met. Our site coordinators not only manage the recruitment of participants, ensuring that they meet the study criteria, but also oversee the enrollment process to ensure it is conducted ethically and efficiently. Furthermore, they are responsible for collecting, recording, and maintaining accurate data throughout the study. This includes ensuring that all data is entered into databases correctly and that it complies with regulatory standards.
Acting as the primary point of contact between the research site and the CRO, they facilitate communication to ensure that all parties are informed about the progress and any issues that arise during the trial. Additionally, they ensure that the site adheres to the study protocol, Good Clinical Practice (GCP) guidelines, and other regulatory requirements. This involves regular monitoring of study activities and resolving any compliance issues that arise.
At SCIRENT, the role of a site coordinator encompasses these general responsibilities with a specific focus on cardiovascular studies, given SCIRENT’s specialization in cardiovascular clinical research. This includes detailed coordination with cardiologists, monitoring cardiovascular-specific endpoints, and managing the unique challenges associated with cardiovascular patient populations.
The impact of SCIRENT’s Functional services extends far beyond the immediate scope of its research projects. By ensuring broad patient access to clinical trials and maintaining the highest standards of research integrity, SCIRENT is playing a critical role in the advancement of cardiovascular health. These efforts not only contribute to the development of new treatments and therapies but also offer hope to patients and families affected by cardiovascular diseases.
How can we help you? We will get in touch shortly.
