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compliance with GxP and all other regulatory agency requirements. The candidate will receive samples from clinical trial sites and enter samples into an electronic database management system. Performs sample
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Maintain rigorous records of experimental progress using electronic laboratory notebooks Qualifications Must-Have Bachelor's Degree and 6+ years of experience or Master's degree and 4+ years of experience
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communication methods (i.e. Email, Video Conferencing, IM) Proficiency in Microsoft (MS) Office and the ability to learn different software programs. Nice-to-Have Minimum of 2 years of relevant work experience in
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communication methods (i.e. Email, Video Conferencing, IM) Proficiency in Microsoft (MS) Office and the ability to learn different software programs. Nice-to-Have Minimum of 2 years of relevant work experience in
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concomitant medications. Supports the implementation and application of electronic health record system (PIMS) in the PCRU. Supports the development of Informed Consent Documents for allocated studies and