Senior Quality & Compliance Lead - Clinical Trials
MMS Holdings Inc.
A leading data-focused CRO is looking for a skilled professional to manage GCP compliance and quality oversight. Applicants should have at least 7 years of experience in a GCP regulated environment and be proficient in audit documentation and project management. Strong communication and problem-solving skills are essential. This role involves maintaining high regulatory standards and may require travel both domestically and internationally. Join a dynamic team dedicated to improving lives through innovative therapies. #J-18808-Ljbffr
Vacancy posted 4 days ago
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