... 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 ...
... 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 ...
... timelines IT proficiency: MS Office, clinical trials systems (e.g. IMPACT, IWRS, ... global patients in Novo Nordisk clinical trials. Working at Novo Nordisk Novo ...
... review and proficient revisions of Clinical Trial Agreements with focus on liability ... , and negotiating confidentiality and clinical trial agreements with CROs and study sponsors · Experience working in a clinical trial setting to include, CRO, site ...
... 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 ...
... working with the physicians within Clinical Development to provide clinical research support for programs as ... at least 5 years as clinical research scientist in oncology are ... ,000 Sites and 675,000+ Trial patients. No matter what your ...
... 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 ...
... UK. Position Summary: The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study ... as needed. Review and query clinical trial data according to the Data ...
... UK. Position Summary: The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study ... as needed. Review and query clinical trial data according to the Data ...
... 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 ...