A clinical research organization is seeking a Senior Regulatory Specialist to provide regulatory oversight for clinical trials. This remote position involves preparing and coordinating IRB submissions, ensuring regulatory compliance, and facilitating training for staff. Ideal candidates will have at least 2 years of clinical research experience along with strong communication and project management skills. Applicants should be able to manage time-sensitive projects effectively while maintaining a high degree of professionalism in interactions.
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Senior Regulatory Specialist - Remote Clinical Trials in houston at Unknown Company
This position is listed as full time and able to be worked remotely.