Senior Clinical Project Manager
... to ensure completion of the Clinical Study Report. Set up and maintain the Trial Master File (TMF), Clinical Trial Management System (CTMS), and other ...
Pozice clinical trial associatepracovník / pracovnice administrativy v obci Pardubice. Vyhledáno 4881 nových nabídek v této lokalitě.
Clinical Operations Manager
... in-quality TA-specific clinical trials through effective management of team to reach CDC CZ trial targets, incl. risk management. Building ... 4 years of experience in clinical trial management (including working as a Clinical Research Associate), with min 2 ...
Start-up Specialist
... performing RA EC submissions of clinical trials and in-depth experience in clinical operation processes and end-to-end clinical trial conduct. Master’s degree in life or natural science. Knowledge of clinical trials. Fluent Czech and English ...
Clinical Systems Implementation Manager
... Note, SharePoint and CoPilot & applicable clinical trial systems such as Veeva Vault. ...
Clinical Supply Chain Manager
... and manage vendors involved in clinical supplies and interactive response technology. You will: Analyze clinical trial protocols and translate requirements to ...
Clinical Operations Specialist
... you. About the Role: The Clinical Operations Specialist works with the Clinical Trial Team to ensure successful study ... and maintenance of studies in Clinical Trial Management Systems (CTMS), ensuring all ...
Clinical Sales Representative Rythm Management
... ) by travelling to identify their clinical needs, goals, and constraints related ... a defined region by providing clinical education, sales strategy and support ... nurse, or product specialist, or clinical specialist, etc.) experience. Biomedical technician ...
Clinical Research Associate - Entry level
... for you Our successful Clinical Research Associates possess varied backgrounds ... regulatory experts Internally designed propriety Clinical Trial Management System - one stop shop ... the protocol; Assessing the clinical research site’s patient recruitment and ...
Senior Regulatory Specialist, EMEA Regulatory Affairs (Clinical Investigation Support)
... to pre- and post-market clinical investigations, as well as all ... to and learning from global clinical investigation submission and strategy experiences. ... or global regulations related to clinical investigations. You have strong time ...
Clinical Research Associate - Experienced
... medical site staff including coordinators, clinical research physicians and their site ... and Local Regulations; Assessing the clinical research site’s patient recruitment and ...