Regulatory position with a top Fortune 500 company- To provide document management and publishing support within NonClinical to enable successful electronic authoring, publishing, delivering, securing and archiving of regulatory submission documentation to worldwide regulatory agencies. Provide electronic regulatory study submission reports using CoreDossier publishing system for delivery to Regulatory Operations. Utilizes experience to ensure assigned work is within the guidelines of departmental policies and procedures. When you work for Smith Hanley Consulting Group , you are partnering with a leader in clinical trials and scientific staffing. For over two decades, we have built solid and successful relationships with top pharmaceutical companies across the USA. Our recruiters are committed to finding you the perfect job, allowing you to build and diversify your experience. We are dedicated to understanding your skills and career goals inside out.
- company: Smith Hanley Consulting Group
- employee_type: Contractor
- full_time: Full Time
- industry: Science, Pharmaceutical & Biotech
- job_title: Document Specialist