... boards, adjudication committees and Safety Data Monitoring boards. In addition, you ... within your project in collaboration associate Head of Medicine. As a Executive Director Clinical Development, you: You author Investigator`s ...
... boards, adjudication committees and Safety Data Monitoring boards. In addition, you ... within your project in collaboration associate Head of Medicine. As a VP Clinical Development, you: You author Investigator`s ...
... global leadership across clinical operations, partnering with data management, regulatory teams, clinical research professionals, and other stakeholders. ... , contractual agreements, and clinical data dissemination. Oversee individual trials, focusing ...
... sponsor dedicated Site Monitor II (Clinical Research Associate II) with at least 3 years of Oncology monitoring experience in Germany. The Site Monitor II will be responsible for data integrity, data quality and ensuring compliance with ...
... and bid defense meetings Lead clinical resources in a matrix environment, as required, including Clinical Trial Assistants and Clinical Research Associates Set expectations for the study ...
... and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement ...
... time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with ... path into Clinical Trial Management (CTM). Responsibilities Communicate ...
... full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with ... status reports within the clinical trial management system Interact with ...
... sites to support the client’s clinical development programs Collaborate with internal ... to work on the client clinical trials Attend key therapeutic trainings ... and related activities in a clinical trial Ability to have scientific ...
... might affect subject safety and clinical data integrity at an investigator site ... and medical records. Verifies required clinical data entered in the Case Report ... skills relating to colleagues and associates, both inside and outside of ...