... . As the Director Medical Affairs Hematology, you will represent Regeneron in Medical Affairs and Clinical Development providing scientific ... across Medical Affairs, Clinical Sciences, Operations, and Regulatory, and provide guidance to Commercial ...
... Director of Clinical Affairs Role Overview : The Director of Clinical Affairs is responsible for driving the strategic direction and execution of the organizations clinical research initiatives, ensuring adherence to international standards and regulatory ...
... regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy ... associate Head of Medicine. As a Executive Director Clinical Development, you: You author ...
... proactive and experienced Quality Assurance & Regulatory Affairs (QA RA) Manager. This role ... considered for this Quality Assurance & Regulatory Affairs Manager: Essential: 4+ years in ... 13485 compliance. Oversee the regulatory strategy for existing and new ...
... strategic clinical development and regulatory affairs (experience in people management is ... not sufficient). Experience working across different pharmaceutical companies and or regulatory authorities (a plus). ...
... and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific ...
As a Start Up Associate II, you will be ... ICH guidelines and other regulatory requirements. This includes effective communication ... preparation of content for Regulatory submissions Handling ICF negotiations and ... BS BA degree or Associates degree with min. of 2 ...
... guidance and expertise to the Regulatory Submissions team in terms of ... processes; Oversee Study Start-Up Regulatory Submission activities and timelines to ... disciplined approach. We leverage local regulatory and therapeutic expertise across all ...
... a full-time, office-based Associate Clinical Trial Manager (aCTM) to ... quality control of our internal regulatory filing system Provide oversight and ... disciplined approach. We leverage local regulatory and therapeutic expertise across all ...
... a full-time, office-based Associate Clinical Trial Manager (aCTM) to ... quality control of our internal regulatory filing system Provide oversight and ... disciplined approach. We leverage local regulatory and therapeutic expertise across all ...