5+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology) * Strong working knowledge of clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies Clinical Research, Clinical Studies, Communication * Planning and execution of pre-/post-market clinical studies (vascular, oncology); ensure deliverables are completed on time and within budget. * Provide regular reporting of metrics to Clinical Affairs leadership. * 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, ...
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