... ). Trains external stakeholders (i.e,. clinical monitors, clinical site personnel) and internal global clinical study teams regarding IMP handling. Files proper documentation throughout the study and after study closure.5. Utilizes Interactive Response ...
... of clinical research study procedures with Abbott EP technologies, ... feedback to Clinical Scientists, study teams, and Clinical Site Leads on study design and procedure and product experiences. Collaborate with Clinical Affairs, Medical Affairs, R&D ...
... ensure timely delivery of quality study data. Study Managers may also input to and support compilation of sections to Clinical Study Reports.Will provide leadership to ...
... through the lifecycle of the clinical study, to ensure an effective clinical study conduction and completion Act in ... interact with QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical Trial Managers (CTMs), Global Regulatory ...
... reports, communications with Clinical Program Managers, study site personnel, and others as ... to budgets, clinical research agreements and informed consents * Develop a familiarity with the protocols, study timelines, inclusion and exclusion criteria, ...
... reports, communications with Clinical Program Managers, study site personnel, and others as ... to budgets, clinical research agreements and informed consents * Develop a familiarity with the protocols, study timelines, inclusion and exclusion criteria, ...
... for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs) Collaborates with Clinical Safety Scientist Product Lead and ... [TFLs]), and other clinical study documents Collaborates with Clinical Safety Scientist Lead and PSL ...
... .LCRAs work with a qualified Study Team of Clinical Research Associates who identify, select, ... to the Project Manager of clinical trials to coordinate all study-related activitiesAssists with other project ...
... global country and site feasibility, clinical study start-up and business operationsExperience in clinical research, including clinical trial conduct, knowledge of GCP ...
... and safety-related sections of study documents together with other DSPV team members and in collaboration with clinical team members.Support the DS ...