2025. 06. 13. | Teljes munkaidõ | Parexel& Responsibilities Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. Assess change controls and provide regulatory assessments of quality changes in production and quality control. Review study reports from the quality
Nézze később2025. 06. 12. | Teljes munkaidõ | Budapest | Parexel& Responsibilities Develop submission strategies and plans for post-approval CMC activities such as variations, renewals, market expansions, and annual reports. Assess change controls and provide regulatory assessments of quality changes in production and quality control. Review study reports from the quality
Nézze később2025. 06. 05. | Teljes munkaidõ | ParexelConcise, selling proposal texts. You will need Ideally Educated to at least Bachelor of Science level or Bachelor of Science in Nursing or Masters, MD, PhD Relevant clinical research experience in management of international clinical trials Prior project leadership, or site-based study coordination
Nézze később