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Clinical Research Coordinator
Provides management and oversight of oncology clinical trials conducted at CalvertHealth. Performs a variety of complex duties to support the conduct of clinical research, such as, facilitating the informed consent process, coordinating required research activities; collecting, compiling, and documenting clinical research data to ensure adherence to protocols and validation of information and documents. Study specific regulatory processes in accordance with appropriate regulations, standard operating procedures and study specific protocols/plans. Promotes the ethical conduct of research and ensures compliance with federal, state and institutional regulatory requirement
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