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doing so, you will also work closely in a matrix-team environment with bioanalytical and ADME scientists to ensure the execution of appropriate experimental plans and data interpretation. You will also
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skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED
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development process, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment Demonstrated success in prior scientific/technical/administrative roles Demonstrated experience
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skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED
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development / reporting, and related visualizations Demonstrated effectiveness working in cross-functional business environment. Proven leadership skills in managing people and projects both directly and via a
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PHYSICAL/MENTAL REQUIREMENTS Ability to work in a laboratory environment performing experiments in a laboratory fume hood. Ability to perform complex data analysis. NON-STANDARD WORK SCHEDULE, TRAVEL
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abilities. Nice-to-Have. Previous QA or QC experience in a regulated industry Previous experience in a field that requires priority on detail management in a self-regulated work environment. Pharmaceutical
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awareness of changing external regulatory environment to ensure this thinking is reflected in the science performed within the function. Represent CRD to ensure good collaboration, proactive engagement, and
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applications including Word Processing, Excel, and PowerPoint Ability to work in a team setting. PHYSICAL/MENTAL REQUIREMENTS Work in a lab environment for the majority of the workday. Work with various types
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editing methods with high-dimensional functional assays and physiologically relevant cell models. He/She/They will collaborate closely with partner lines in a highly cross-matrixed environment to develop