Perform role as a Principal Investigator on Good Laboratory Practice (GLP) and non-GLP non-clinical studies. Review physiological data such as cardiovascular, central nervous system, and respiratory data acquired via telemetry or hard-wired system to create tabular, graphical, and/or reports for customers and internal studies. Assist the computer system validation specialist in the development of IQ/OQ Test scripts, , traceability matrices, and validation summary reports.

Essential Duties And Responsibilities

• Generate study plans and reports for delegated phases of the non-clinical study.
• Review, analyze and report physiological data acquired from various software platforms
• Gain expertise on cardiovascular, central nervous system, and respiratory physiology
• Attend and actively participate in external scientific meetings
• Identify and resolve technical issues and propose solutions

Education And Experience Required

Bachelor’s Degree in biomedical engineering, biological science or related medical/scientific experience considered.

Skills And Abilities Required

• Excellent communication, organization skills, and ability to work closely with internal and external customers.
• Must possess excellent problem-solving skills.
• Highly skilled and proficient with Microsoft Word, Microsoft Excel, Microsoft Outlook, and Windows Operating Systems.
• Must be able to learn and become proficient with additional specialized computer software programs.
• Works with minimal supervision with wide latitude for independent judgment.
• Familiarity and/or proficiency with DSI software and technology is highly desired.

Bonus Skills & Experience

Preferable experience using the DSI Software or working in an academic lab or pre-clinical lab. Experience working under GLP regulations for conductance of non-clinical studies. Computer programming knowledge (VBA, Matlab, R, etc.).