Do you want to be part of a dynamic team, working in an international environment that drives clinical trial activities? Would you like to be involved in the planning of a trial portfolio on a strategic level? Then keep reading \xe2\x80\x93 we may have just the right job for you! Novo Nordisk Malaysia has opened a role for a Feasibility Specialist, join us and apply today!
About the department
The Clinical, Medical, Regulatory and Quality (CMRQ) department is one of the key functions that enable the business strategy through the effective execution of functional goals, in the areas of Clinical Research, Medical Affairs, Regulatory, and Quality Assurance. The position of Feasibility Specialist is to be in Kuala Lumpur, the capital of Malaysia, and report to the Clinical Operations Manager.
The position
The successful candidate will conduct a data-driven review and site feasibility for studies including inputs to protocol design (if relevant), following the currently proposed Global Trial Planning (GTP), with International Conference on Harmonization-Good Clinical Practice (ICH-GCP), and with the applicable regulatory requirement(s).
The position tasks are, but not limited to:
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