Clinical Research Associate (m/w/d), Single Sponsor
... of one year of on-site monitoring experience * Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference ...
... of one year of on-site monitoring experience * Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference ...
... educational equivalent Experience in on-site monitoring of clinical trials Alternatively, you should have ...
... of one year of on-site monitoring experience * Knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference ...
... the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference ...
... educational equivalent Experience in on-site monitoring of clinical trials Alternatively, you should have ...
... the project team and study sites; Collaborate with and coordinate site investigators ensuring overall integrity of ... ; At least two years of clinical trials related experience (as investigator, ...
... service providers (couriers). Station Operations Managers are the right hand person for the Site Leaders and will lead the ...
... area managers, chief engineers, facility technicians.· Establish performance benchmarks, conduct analyses, and prepare reports on all aspects of the critical facility operations and maintenance· Responsible for the on-site management of shift technicians ...
... service providers (couriers). Station Operations Managers are the right hand person for the Site Leaders and will lead the ...
... team as Cluster Loss Prevention Manager. In this key role, you ... to a cluster of operational sites across the end-to-end ... as a service to operational sites from across the Amazon supply ...