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Clinical Information Associate
The clinical data you will be evaluating is on the safety and efficacy of our (and our competitors) groundbreaking heart valve which has the potential to replace traditional open heart surgery for the treatment of heart valve disease. Day to day activities will include reviewing, analyzing and summarizing clinical data, interacting with international key opinion leaders and investigators in the field, assisting in preparing data presentations for major meetings and manuscripts for peer reviewed medical journals, conducting literature searches, assisting in the preparation of literature reviews, assisting with the conducting of internal training on the clinical data and cross functional teamwork with our data management, marketing and research and development partners.
Requirements: *Multi-level position: Position title and level posted is preferred. However, depending on experience, we will also consider hiring at the Clinical Information Associate level.
• Requires hands-on clinical research experience encompassing all aspects of the clinical process as follows: A minimum of two years monitoring/data management/marketing experience for the Clinical Information Associate level and four years monitoring/data management/marketing experience for the Sr. Clinical Information Associate level. Ideal candidate will have four years experience in clinical research with at least two years of field monitoring experience within the medical device industry. Desired experience includes knowledge of interventional coronary or peripheral products such as stents, open or minimally invasive cardiac surgery or other class III devices. Experience working with key opinion leaders/investigators desired. Prior experience in presentation preparation a plus.
• A bachelor's degree is required. A degree in a biological or life science discipline or nursing desired.
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