Clinical Trials Regulatory Specialist
Automatic Data Processing
Automatic Data Processing, Inc. in Springfield, NJ is seeking a Regulatory Associate to support clinical trials by preparing and submitting regulatory and IRB documentation across multiple studies.
You will work with Investigators, Sponsors, CROs, IRBs, and other stakeholders to ensure compliance with GCP, ICH, HIPAA, sponsor requirements, and company SOPs. The role emphasizes coordination of submissions, regulatory binders, and communication to keep study timelines on track, with strong
#J-18808-LjbffrVacancy posted 4 days ago
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