Director Clinical Affairs
... Responsibilities : Establish and execute clinical affairs strategies aligned with regulatory and business objectives. Foster relationships ...
... Responsibilities : Establish and execute clinical affairs strategies aligned with regulatory and business objectives. Foster relationships ...
... 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 ...
... with internal colleagues across Medical Affairs, Clinical Sciences, Operations, and Regulatory, and provide guidance to Commercial ... and external stakeholders. Representing Medical Affairs for Hematology at cross-functional ...
... 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 ...
... 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 ...
... 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 ...
... Site Monitor II (Clinical Research Associate II) with at least 3 ... Responsibilities and Study Conduct Ensuring regulatory, ICH-GCP and protocol compliance. ... skills relating to colleagues and associates, both inside and outside of ...