Planning and execution of pre-/post-market clinical studies (vascular, oncology); ensure deliverables are completed on time and within budget. * Develop Clinical Investigation Plans (CIPs), Informed Consent Forms (ICFs), Study Management Plans, Case Report Forms (CRFs), and support the creation and maintenance of full clinical study documentation. * Review and provide input on the development of other essential clinical study documents related to clinical data management, clinical statistics, site management & monitoring, clinical safety management, clinical product management, and clinical supplier management. * Compile regulatory dossiers and submit clinical studies to Ethics Committees (ECs) and Competent Authorities (CAs) in the European Union, the United Kingdom, and Switzerland. Communicate with ECs and CAs on all study-related questions and obtain approvals required to conduct the study.
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