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Job description
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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Worksite address
houston, TX, 77246, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.