Stellenangebote für Clinical Monitor Jobs in Saarland Bundesland

Top Job | Vollzeit | Penzberg | Roche Diagnostics GmbH

Tightly integrated with bioinformatics specialists our group performs statistical analyses for discovery - validation of new targets and biomarkers, monitoring drug effects, as well as elucidating the mechanism behind diseases. In this environment, your main responsibilities include but are not limited to

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Top Job | Vollzeit | Berlin | Immutep GmbH

Study specific documents; i.e. safety management plan, medical monitoring and medical review plan, statistical analysis plan, IDMC/DSMB charters etc. Manage and liaise with investigators, key opinion leaders and study groups in the light of ongoing clinical trials Evaluate internal and external clinical

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20.05.18 | Vollzeit | Baden-Baden

Als Qualification Specialist zur Software- und Dokumentenkontrolle PerkinElmer LAS (Germany) GmbH Ingelheim am Rhein Monitoring von Audit-Trails verschiedenster Geräte- und Softwaretype. Partner-Anzeige 55218 Ingelheim (Rhein) 17.05.2018 Chemielaborant (m/w) in der Wasseraufbereitung Widmann Ges. für

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Top Job | Vollzeit | München | GermanPersonnel e-search GmbH

Development of new employees, e.g. co-monitoring Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs

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Top Job | Vollzeit | Berlin | Immutep GmbH

Documents; safety management plan, medical monitoring and medical review plan, statistical analysis plan, IDMC/DSMB charters etc. Manage and liaise with investigators, key opinion leaders and study groups in the light of ongoing clinical trials Evaluate internal and external clinical trial data Present key

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Top Job | Vollzeit | Frankfurt am Main | GermanPersonnel e-search GmbH

CRA will be assigned clinical monitoring activities in a single country or in several countries ensuring quality service and appropriate clinical study conduct. The Senior CRA shall guarantee the adequacy, the reliability and quality of the data collected from sites and shall participate in the

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