, sponsorship, networking, focused leadership development and dynamic real world work experience. Global Trial Associates (GTAs... and/or country feasibility. Collaborates with the Global Project Team, e.g. Clinical Trial Manager (CTM)/Global Trial Lead (GTL...
and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial... Management team in our Seoul, South Korea office. The aCTM will be a part of the Clinical Trial Management team and support...
and/or Post-Doctoral Research experience for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial... Management team in our Seoul, South Korea office. The aCTM will be a part of the Clinical Trial Management team and support...
and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM... Trial Management (CTM). Responsibilities : Communicate and collaborate on global study activities; working closely with the...
and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM... Trial Management (CTM). Responsibilities Communicate and collaborate on global study activities; working closely...
), Clinical Research Associate (CRA) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the...About the job: Local Trial Management services provides local management of a clinical trial (or Medical Affairs data...
Purpose of the Job The Study Start-Up Associate Director (SSU AD) is responsible at country level for organizing... and other applicable procedural documents and process improvement Has excellent understanding of the local clinical trial environment...
Study Start Up Associate II-Home Based-South Korea-ICON Strategic Solutions ICON plc is a world-leading healthcare..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Study Start Up Associate II...
. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate (CRA...
of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research Associate II...
. Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory..., and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Clinical Research Associate (CRA...
Job Summary : We are currently seeking a full-time, Senior/Principal Clinical Research Associate to join our Clinical..., the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial...
Job Summary We are currently seeking a full-time, Senior/Principal Clinical Research Associate to join our Clinical... are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial...
Job Summary : We are currently seeking a full-time, experienced Clinical Research Associate to join our Clinical..., the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial...
Job Summary We are currently seeking a full-time, experienced Clinical Research Associate to join our Clinical... are protected, the reported trial data are accurate, complete, and verifiable from source documents, and the conduct of the trial...
Short Role Description The Local Study Associate Director (LSAD) is responsible for managing their assigned clinical.... This role reports to DCH or DSMM, depending on country-specific organisational set-up and works in alignment with Global Study...
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare... and regulatory on safety issues if necessary. Responsible for appropriate communication between product safety locally, Global...
the site staff and principal investigator with support as needed on the goals of the clinical trial program, protocol..., and patient treatment principles for the trial ensuring a trusted partnership. Conducts site evaluation, site training, routine...
the site staff and principal investigator with support as needed on the goals of the clinical trial program, protocol..., and patient treatment principles for the trial ensuring a trusted partnership. Conducts site evaluation, site training, routine...
of contact on quality and compliance matters to the SMM Oncology Country teams for high-quality clinical trial delivery. Drive... in quality compliance. Share global process updates impacting local SMM team quality compliance in a timely manner. Facilitate...