Clinical Study Manager
... for the duration of the study. Works together with Regulatory Affairs ... by ICH-GCP prior to study start have been collected and ... . Sets up and maintains the study in CTMS at study country level as well as ...
... for the duration of the study. Works together with Regulatory Affairs ... by ICH-GCP prior to study start have been collected and ... . Sets up and maintains the study in CTMS at study country level as well as ...
... as coordination and tracking of study materials and equipment Ø Assist in ... for the duration of the study Ø Set-up and maintenance of ... the eTMF “Inspection Readiness” and study documents are ready for final ...
... a leader of the Study Start-up team you will ... in other facets of Study Start-up are welcome. Responsibilities ... standard operating procedures and study protocols; Provide input on new ... preferred +10 years of Study Start-Up leadership experience within ...
... and healthcare community. As the Director Medical Affairs Hematology, you will ... , reporting to the Senior Medical Director DACH, and leading a dedicated ... closely with the Country Medical Director and Global Medical Directors in the US. Leading the ...
... key business stakeholders (e.g., study teams) to support timely completion ... for assigned region during the study start up period Building relationships ... activities Leading the preparation of study level essential document templates Aiding ...
Job Description Job Title: Executive Director Clinical Development - Oncology Tasks & ... of Medicine. As a Executive Director Clinical Development, you: You author ... of English language The Executive Director Clinical Development role additionally requires: ...
... pre-award and post-award study feasibilities, build and maintain strategic ... and holding meetings with network directors Conducting regular performance reviews for sites participating to our studies, ensuring quality study delivery Serve as an escalation ...
... Clinical Affairs Role Overview : The Director of Clinical Affairs is responsible ...
... clinical aspects of the study. What you will be doing: ... CRAs, drives enrolment and study start-up activities, reviews trip ... Set expectations for the study team and drive a performance ... clinical deliverables of a study Subject matter expertise in the ...
... a key role in the study start-up and clinical trial ... . Responsibilities Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document ...