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compliant study design and execution. Collaborating with clinical, safety, CMC, and other cross-functional teams to ensure... and regulations. Excellent written and verbal communication skills, with high attention to detail and accuracy. Ability to work...
. As a Global Study Associate, you’ll support the delivery of clinical studies in early oncology. You’ll provide key administrative.... What you will be doing Collect, review, and track study documents. Help set up, maintain, close, and archive the Trial Master File (TMF...
and expand these research activities, the group is seeking a Study Coordinator. Our research is built around the identification.... Knowledge of GCPs, in the context of clinical trials. Ability to work independently and as part of a team. Main...
, with a strong service-oriented and client-focused mindset. Ability to work effectively as part of a team. Advanced level of Microsoft... learning and a wide range of responsibilities within a stimulating work environment. Individual training opportunities...
. Prepararing and monitoring of the specimens included in the study. Skilled execution of research protocols. Collaboration... developed. Continuous learning and a wide range of responsibilities within a stimulating work environment. Individual...
. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study... lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...
prototypes for new products, shelf-life study, lab trials and formulation tweaking as per guidelines. Operate lab/kitchen.... We foster innovation and team work, and we care for health and sustainability, which is at the center of our strategy...
in accordance with the requirements of the program-specific V&V plans in a technical work environment with continuously increasing... with timescales and milestones Open minded to offer new ideas for improving processes and tools. Available for travel...
with protocols and regulatory requirements. Maintain and organize clinical trial documentation, including study files, essential... documents, and regulatory submissions. Support the preparation of study-related materials, such as informed consent forms...