As an equal opportunity employer, iCAD values the strength that diversity brings to the workplace. We offer our employees an exciting work environment, competitive salaries and a comprehensive benefits package that includes medical and dental insurance, life and disability coverage, a 401K plan and more.

CLINICAL SITE COORDINATOR

The Company

iCAD, Inc. (Nasdaq: iCAD) is an industry-leading provider of Computer-Aided Detection (CAD) solutions that enable healthcare professionals to better serve patients by identifying pathologies and pinpointing cancer earlier. iCAD offers a comprehensive range of high-performance, upgradeable CAD systems for the high, mid and low volume mammography markets. iCAD is entrusted with the task of early cancer detection by over one thousand women's healthcare centers worldwide. For more information, call +1 877 iCADnow or visit www.icadmed.com

Position Description

Responsible for all activities necessary to commence, conduct, manage and close-out data collection with collaborative research sites. Support Engineering, Software Engineering, and Quality Assurance through the collection, processing, and maintenance of data.

Responsibilities:

• Develop and maintain relationships with collaborative research sites to provide research and development data
• Ability to act as the principle investigator
• Manage Institutional Review Board (IRB) processes or contracts to ensure receipt and approval with clinical partners
• Prepare applications and amendments to the IRB and contract documents for all new and existing proposals
• Develop and maintain data collection protocols in cooperation with QA to ensure adherence to Standard Operating Procedures (SOP), protocol guidelines, Good Clinical Practice, FDA regulations and HIPAA compliance
• Develop budgets and timelines for new projects
• Participate in development of protocols for new projects
• Assist with setup of the databases and creation of data management guidelines for new and existing projects
• Frequently travel to clinical sites to collect research data
• Collaborate with internal team members to determine future research and development data requirements.
• Work closely with Engineering and Software Engineering to ensure data integrity.
• Catalogue internal research data.

Requirements

• Associate's degree or equivalent work experience required
• Knowledge of FDA and HIPAA regulations
• Excellent oral and written communication skills
• Proven ability to communicate technical data requirements to non-technical clinical staff
• Relationship building skills

DESIRABLE

• Knowledge of Matlab
• Knowledge of C++, Java or C#
• Knowledge of one or more scripting languages
• Develop and maintain software tools to view and manipulate research data.

Compensation- iCAD offers a competitive salary with a comprehensive benefits package including Health, Dental, Short Term Disability, Long Term Disability, 401k, Section 125 Health and dependant care accounts and Company provided Life.

Location:This position will be based out of our Beavercreek, OH office

Contact: Please forward cover letter, resume and salary requirements to hr@icadmed.com for immediate consideration.

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