Our client is a professional Medical Devices organization, based in Noord-Brabant Netherlands.
A internationally operating and manufacturing Medical Devices Company
As a CPM you will be responsible for overseeing the development, implementation and execution of several clinical studies. The successful CPM will demonstrate expertise in all areas of clinical study development and execution.
As a CPM you will assess priorities and make assignments to direct reports
You will develop and implement project plans and resource requirements
As a CPM you will ensure that clinical study teams fulfill their responsibilities in accordance with scope of the project plan and with corporate standards, regulations and GCPs
You will coordinate the development of clinical study reports for submission of regulatory authorities
5+ experience in medical device/ivd or pharma
2+ experience in a managerial role
knowledge of ICH-GCP
knowledge of regulatory legislation
English (speaking an writing)
good understanding of the compliance framework for medical interactions in relation to the applicable regulations, codes of practice and SOPs
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