Clinical Research Online Course
Feasibility assessment is a critical step in conducting a successful clinical trial. Selecting the right site can be beneficial for both the sponsor and the clinical site. In addition, it can provide an opportunity for many patients to be enrolled in a study that may change their life. Therefore, the…
According to the FDA website, Real-World Data (RWD) is the data relating to patient health status and/or the delivery of health care, routinely collected from a variety of sources. RWD can come from a number of sources including Electronic Health Records (EHRs), claims and billing activities, product and disease registries, patient-generated data…
If you are looking for clinical research positions and have no experience in terms of clinical trial management systems (CTMS), in this article you will be able to understand how this system facilitates the process of monitoring. Before moving to how the CTMS helps the clinical research associate (CRA), let’s…
The very first step of conducting a clinical trial is to find the right clinical site and Principal Investigator (PI). Sponsors or CROs usually have specific criteria for selecting a site based on the study design and protocol. There are several ways that sponsors find potential clinical sites before conducting…
In traditional trial designs, a single drug is tested in a single disease population in one clinical trial. In contrast to traditional trial designs, master protocols, use a single infrastructure, trial design, and protocol to simultaneously evaluate multiple drugs and/or disease populations in multiple substudies, allowing for efficient and accelerated…
A Note to File (NTF) is a record that allows the clinical site and the sponsor to document an identified issue or discrepancy during a clinical study. A NTF should include the following items: · The root cause of the discrepancy/issue · The corrective action taken to prevent its recurrence · Explanation of…
The Informed Consent Form (ICF) is one of the documents that is reviewed by the CRA during the monitoring visit. It is the CRA responsibility to ensure that the patient (subject) has been consented, appropriately. If the consent is not signed or completed properly, additional training for the Clinical Research…
For all clinical trials involving human beings, informed consent is mandatory however, in certain conditions the IRB might waive the informed consent. The Clinical Research Coordinator (CRC) and Clinical Research Associate (CRA) are two major roles in clinical research that deal with consent forms. In this article I will discuss…
Clinical Research Associates (CRAs) have several responsibilities. Source Data Review (SDR) and Source Data Verification (SDV) are the most common tasks that CRAs perform during a monitoring visit. SDV is basically conducted to compare Case Report Form (CRF) to source data. SDR is a review of source documentation to check quality…
Base on ICH-GCP guidelines Institutional Review Boards (IRBs) are responsible for conducting ethical review of the study protocol. In clinical trials, patient safety is the first priority and therefore IRB responsibility is to make sure that the study protocol is ethical and the study staff/PIs are well trained and qualified…