The Sr. Clinical Research Coordinator will be responsible for overseeing and managing clinical research studies, ensuring compliance with protocols, obtaining informed consent, and coordinating clinical trials. The role involves collaboration with investigators, research staff, and participants to ensure the successful execution of research projects. Additionally, the coordinator will maintain accurate and detailed records, adhere to regulatory requirements, and manage study documentation.
Qualifications
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Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the medical product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice ...