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Job #02319

About our client Our client focuses on providing mechanical means for treatment of heart failure. The development-stage medical device company, founded in the late '90s, has entered early human trials with its initial device and intends to pursue a family of products to expand the capabilities and applicability of its product platform. Position Location Site Manager Illinois Salary Highly competitive package, commensurate with experience Responsibilities 1) Assist with the development of clinical protocols and CRFs for using in clinical trials 2) Handle assigned accounts along with supporting other accounts 3) Select and qualify sites 4) Assist sites with contracts/budgets/investigator agreements and consents for pivotal trial 5) Initiate site and participate in physician training 6) Train and educate coordinators, physicians and support staff 7) Build relationship for the entire research team 8) Support on-site case 9) Ensure enrollment goals are met 10) Monitor CRF, etc. 11) Support all product lines globally 12) Coordinate and interpret clinical studies and user preference registries, market surveys 13) Support and train customer and in-service medical teams 14) Develop product champions 15) Assist customers with publications and presentations at meetings 16) Provide educational support to the customer base to include the development of training and marketing materials 17) Conduct medical/clinical research with regard to patient populations and competitive products 18) Support the company in sales after the products are approved for marketing release 19) Support research and development by gathering information from the medical community and communicate this information to the engineering team 20) Follow up and track customer complaints according to established procedures for reporting such information to the corporate office Requirements 1) Degree in Nursing, Medicine or Biomedical Engineering with a focus on clinical 2) 5 years of experience in either cardiac surgery or cardiology 3) 3 years of experience in industry with medical device technology, clinical trial research background 4) In-depth knowledge of GCP guidelines and FDA requirements 5) Strong project management capabilities/clinical trial monitoring experience a plus 6) Experience in educating and training physicians and hospital support staff in the critical-care arena, catheter lab and/or operating room 7) Excellent written, oral and interpersonal communication skills 8) Superb problem-solving skills 9) Willingness to travel – up to 75%