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This question is about what a clinical scientist does and clinical scientist.
What is a clinical scientist in pharma?
A clinical scientist in pharmaceuticals performs a critical function in the clinical development of pharmaceutical products. This function is involved with every step of clinical trials, from the conception to the read-out, market approval filing, to publication.
Therefore, clinical scientists who work in the function play a major role in and greatly impact clinical trials. Clinical pharmaceutical scientists ensure that medicines are safe to use and are prepared and dispensed in an aseptic environment.
Clinical scientists are primarily responsible for setting up and monitoring clinical trials. This involves collaborating with trial investigators and training the clinical trial sites. In addition, clinical scientists are responsible for writing clinical protocols, monitoring data, and reporting safety-related events.
Clinical scientists work on interventional clinical trials across different disease settings such as cancer, infectious disease, immunological diseases, cardiovascular disease, and many more.
In addition to interaction with the study responsible physician, clinical scientists also interact with professionals from other pharma functions. These include biomarker leads, safety scientists/physicians, project management, medical writers, statisticians, regulatory scientists, and other clinical trial leads and associates.
External to the pharma company, clinical scientists play a critical role in coordinating and communicating trial information to the investigators who advise and recruit patients for clinical trials.
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