As Clinical Study Managers, we oversee the planning, implementation, and management of clinical trials in accordance with regulatory requirements and guidelines. We coordinate multiple aspects of clinical trials, including recruitment, data collection, and compliance with protocols. Our role involves close collaboration with various stakeholders such as investigators, clinical research associates, and regulatory agencies. We ensure that trials are conducted efficiently, within budget, and adhere to ethical standards. Our work is crucial to the development and approval of new medical treatments and therapies.
Core tasks:
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