Clinical Site Manager
... to work on the client clinical trials Attend key therapeutic trainings meetings ...
... to work on the client clinical trials Attend key therapeutic trainings meetings ...
... ensure Good Clinical Practice (GCP) and regulatory compliance. Support pharmacovigilance efforts to ensure safety reporting and manage safety signals throughout the trial. Contribute to business development efforts, participating in project bid proposals ...
... main point of contact for project teams regarding site performance issues ... ; Minimum 1 years site and clinical trials experience (more experience for the ...
... critical paths and discuss with Project Controls Manager for resolution Establish all equipment ... to their schedule commitments. Project Trend and Change Management Once ... areas of potential concern. Project Progress Measurement and Earned Value ...
... with primary Site Manager who will act as the primary liaison with site personnel. Prepares for and attends Investigator Meetings and sponsor face to face meetings. Participates in global clinical monitoring and project staff meetings (inclusive ...
... upon Manage the delivery of project management team outputs, in accordance with agreed timescales and quality standards Mentorship of junior project managers Qualifications Minimum Requirements Academic or ...
... deliverables: tracks progress of the clinical trial, manages study data, budget, investigational ... ). 0 -2 years of relevant clinical trial experience with associated skill sets. ...
... . We are looking for a Project Procurement Manager (f m d) to join ... , e.g. as technical buyer, project procurement manager buyer or category manager Relevant experience in complex procurement, ...
... and Essen . As a Consultant Project Engineer , you will be responsible ... with diverse stakeholders. Experience with project management tools and methodologies. Analytical ... become part of a visionary project that will have a direct ...
... role in designing and analyzing clinical trials, interpreting complex medical data, and ... years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP ...