... hire and lead teams and coordinators, champion program excellence, and ensure ... 120 days prior to the coordinators end-of-term agreement and ... values; reinforce core values with coordinators. Foster an environment in which ...
... relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge ...
... relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge ...
... be responsible for aligning the clinical strategy and execution plan with ... external partners, including universities, CROs (Clinical Research Organizations), and capsules products ... asset. The ability to align clinical strategies and development efforts with ...
... early phase development, delivering successful clinical trials and contributing to medical and ... Affairs – ideally you also supported clinical trials in that role. Solid and ...
... impact the delivery of our clinical trial programs in a company that ... the resources assigned to the clinical trials. You will oversee the budgets ... methods processes of delivering quality clinical trials with reduced budget and in ...
... Review Board (IRB) submissions Manage trial master files, budgets, and agreements ... of study databases for managing clinical data Monitor and analyze clinical study data and report on ... FDA) laws and guidance on clinical studies Strong working knowledge of ...
... understanding and working knowledge of clinical research, phases of clinical trials, current GCP ICH & country clinical research law & guidelines. Excellent understanding ... and training programs related to clinical trials, therapeutic areas, hard and soft ...
... timelines IT proficiency: MS Office, clinical trials systems (e.g. IMPACT, IWRS, ... Poland is responsible for conducting clinical trials across this group of countries, providing clinical trial management and administration support to ...
... timelines IT proficiency: MS Office, clinical trials systems (e.g. IMPACT, IWRS, ... global patients in Novo Nordisk clinical trials. Working at Novo Nordisk Novo ...