Clinical Quality Manager
... expertise to operational team on clinical quality acting as GCP and Novo Nordisk’s Clinical Trial SOPs expert within the CDC (Clinical Development Center Poland). Your will ...
... expertise to operational team on clinical quality acting as GCP and Novo Nordisk’s Clinical Trial SOPs expert within the CDC (Clinical Development Center Poland). Your will ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA lifecycle submissions (e.g., ...
... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA lifecycle submissions (e.g., ...
... , clients and vendors Assess risks associated with clinical product management and quality incidences reported by vendors Support business development tasks related to clinical trial supply services Qualifications College or ...
... (eTMF, CTMS, SSU, Payments) for clinical trial management from site selection to ... Sciences industry with exposure to Clinical Trials and affinity to technology. Experience ...
... to the Director of the Clinical Performance Team, the Associate Medical Director - Clinical Performance will serve as a ...
... already completed Experience in supporting clinical trials at a biotech or pharmaceutical ... already completed Experience in supporting clinical trials at a biotech or pharmaceutical ...
... administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including: Maintaining up-to-date ... medical profession Good knowledge of clinical trials, combined with in-depth knowledge ...
... , and problem-solve. As a Clinical Data Associate Clinical Data Manager I at Rho, you will have the opportunity to collect, process and clean clinical trial subject data. Our Data Management ...
... , and problem-solve. As a Clinical Data Associate Clinical Data Manager I at Rho, you will have the opportunity to collect, process and clean clinical trial subject data. Our Data Management ...