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Clinical Research job

A List of Common Logs in Regulatory Binder

Based on ICH-GCP guidelines definition, essential documents are ā€œthose documents that individually and collectively permit evaluation of the conduct of a trial and the quality of the data producedā€. In order to successfully manage a clinical trial, it is critical to file the essential documents in a timely manner. The…

Local labs and Central labs in Clinical Trials

Several clinical trials require specific lab tests. Depending on the study protocol the lab tests are required to establish inclusion and exclusion criteria, monitor the safety of the patients enrolled in the study or demonstrate the efficacy of the investigational product (IP). The sponsor/CRO has two options for gathering clinical…

Are you planning to enter the clinical research field and you donā€™t have experience in clinical research software? Here are some tips to help you

If you are planning to enter clinical research field and you don’t have experience working with the software used in this area you donā€™t need to be worry. Remember the first time you had to start working with a new software, how did you learn about it? training? watching videos on Youtube?…