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Clinical Study Managers
The Clinical Study Manager is responsible for the day-to-day operations for one or multiple clinical trials. The Clinical Study Manager serves as the trial leader and provides direction to the clinical team to support the overall goals and requirements of the clinical site and sponsors. The Clinical Site Manager drives and manages the clinical study by setting the objectives, scope, strategy and schedule, all the while ensuring that all clinical trial processes adhere to Good Clinical Practices as well as other imposed regulations and guidelines.
This is a hands-on role in any clinical site, so a four-year degree in life sciences is required in addition to extensive experience in a clinical research environment. Excellent communication skills are critical as well as a comfort level with discussion and viewing medical procedures.
Employment Outlook
Career opportunities for Clinical Study Managers are found in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, sectors of the government, and specialty disease centers and pharmaceutical and medical device suppliers. With the rapid growth of the healthcare industry, Clinical Study Manager positions are expected to increase 14% or more in the next 10 years.
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