2024. 06. 03. | Teljes munkaidõ | Kecskemét | PharmiwebInvestigator in studies Contribute to the study feasibility assessments and bidding process Monitor safety and wellbeing of patients enrolled into our studies Provide medical support
Nézze később2024. 06. 03. | Teljes munkaidõ | Kecskemét | PharmiwebFor and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we’re able to create a place where everyone feels like they belong. Job responsibilities Responsible for site management oversight, clinical monitoring, and central
Nézze később2024. 06. 03. | Teljes munkaidõ | Kecskemét | PharmiwebOf protocol/consent documents/safety reports for Ethics/IRB approval according to local requirements. Pre-study/placement and initiation visits. Conduct regular monitoring visits in accordance with the ICON site monitoring SOP/Sponsor site monitoring SOP/WP as tain all files and documentation
Nézze később2024. 06. 03. | Teljes munkaidõ | Kecskemét | Pharmiwebmonitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned Responsible for all aspects of site management as prescribed in the project plan Ensure the study staff who
Nézze később2024. 06. 03. | Teljes munkaidõ | Kecskemét | Pharmiwebmonitoring plan, study specific training documents. • Supports and contributes to Clinical Study Teams (CSTs) - Trial Management Teams (TMTs) as applicable, agenda driven, present at meetings. • C o mm un icates country status (including timelines and deliverables) to key stakeholders (e.g., Global Clinical
Nézze később2024. 06. 02. | Teljes munkaidõ | Bács-Kiskun | IntsolutionVillamosipar területén világelsőként működő multinacionális partnerünkhöz keresünk BESZERZŐmunkatársatA feladatok sokszínűségében nem fogsz csalódniAz ellátási és készletgazdálkodási paraméterek meghatározása és folyamatos monitorozásaA termelésben felmerülő igények és erőforrások egyensúlyának
Nézze később2024. 06. 01. | Teljes munkaidõ | Kecskemét | PharmiwebAnd motivated individual to join our team as a Polish Clinical Research Associate (CRA). If you are passionate about contributing to clinical research and have a strong background in the field, we invite you to apply. Responsibilities Study Monitoring Conduct on-site and remote monitoring visits to ensure
Nézze később2024. 06. 01. | Teljes munkaidõ | Kecskemét | PharmiwebAnd motivated individual to join our team as a Romania based Clinical Research Associate (CRA). If you are passionate about contributing to clinical research and have a strong background in the field, we invite you to apply. Responsibilities Study Monitoring Conduct on-site and remote monitoring visits
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