Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
September 25
Analytical Instruments • Laboratory Supply Chain Programs and eCommerce • Laboratory Equipment • Lab Services • Specialty Diagnostics
• Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information. • Contribute to site selection, involved in review and approval of study protocols and amendments. • Ensure medical validity of each individual primary endpoint as well study subject safety. • Controls, handles and follows day to day activities during the course of the clinical trial.
• Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important. • Is fluent in spoken and written English. • Shown understanding and experience with NDA submission process. • Shown understanding of regulatory guidelines for adverse event reporting. • Strong communication & presentation skills and is a strong teammate.
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