... company’s new digitalized Clinical & Medical Affairs processes. You will ... in planning & implementing clinical studies in the EU and the US (project management, creating protocols and study documents, sit management, monitoring, audit, ...
... in all assigned cross-functional clinical study teams and other projects and ... other disciplinesProvide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and ...
... in all assigned cross-functional clinical study teams and other projects and ... other disciplinesProvide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and ...
... in all assigned cross-functional clinical study teams and other projects and ... other disciplinesProvide statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents, and ...
... 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 ...
... in all aspects of clinical study planning and startup (including budget ... executing the complete range of clinical study activities, from startup through final study report. Medical devices clinical trial management experience desirable. Experience ...
... client project teams.The Senior Clinical Data Manager role is a ... quality data with compliance to study model procedures and standards; give ... or experience in support of study deliveryYour profileUniversity college degree (life ...
... the headquarters. The Executive Assistant will provide a full range ... . We at PLU Top Assistant think this is an exciting ... for a loyal (Junior-)assistant who is forward-looking and ... this global contribution as Assistant to the Managing Director? Then ...
... contribute to set up of clinical trial related documents and you’ll mange clinical biomarker projects within quality, timeline, ... MD or equivalent degreeSpecialist in clinical genomics with excellent hands-on ...
... contribute to set up of clinical trial related documents and you’ll mange clinical biomarker projects within quality, timeline, ... MD or equivalent degreeSpecialist in clinical genomics with excellent hands-on ...