... of EU clinical trial applications for the EEA region for internally managed trials. The CTSC collaborates with global ... submissions or multinational clinical trial submissions under the EU Clinical Trial Directive. Demonstrated experience being solutions ...
... navigate the complex world of clinical trials to bring life-changing therapies ... with the TMF Lead Project Specialist to follow-up on country ... . TMF and cooperates with TMF Specialist and PS (Project Specialist) TMF Lead to ensure inspection ...
... with all applicable regulations. Ensure clinical trials are performed in accordance with ... other global regulatory requirements governing clinical research. Global clinical trial oversight required Excellent verbal and ...
... with all applicable regulations. Ensure clinical trials are performed in accordance with ... other global regulatory requirements governing clinical research. Global clinical trial oversight required Excellent verbal and ...
... growth Join us as a Clinical Trial Administrator at our recently established Clinical Development Center (CDC) in Poland. ... quality IT proficiency: MS Office, clinical trials systems Fluency in Polish and ...
... candidates into clinical development and drive the development strategy, the design of clinical trials, and contribute to the execution of the clinical development plan in support of ... medical input into clinical trial documents including but not limited ...
... candidates into clinical development and drive the development strategy, the design of clinical trials, and contribute to the execution of the clinical development plan in support of ... medical input into clinical trial documents including but not limited ...
... pressures, and increasing complexity in clinical trials are j The CRO market ... , it’s predicted that the global clinical trials market will hit a value ... lives. Our ‘Own It The Clinical Trials Assistant (CTA)assists in the ...
... candidates into clinical development and drive the development strategy, the design of clinical trials, and contribute to the execution of the clinical development plan in support of ... medical input into clinical trial documents including but not limited ...
... of investigational drugs across multiple clinical trials, accounting for study requirements, patient ... record of successfully managing complex clinical trials. • In-depth knowledge of clinical trial drug supply management principles, GMP ...