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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY We are seeking a chemical engineer/chemist to join
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY We are seeking an experienced process safety
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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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technical staff members on your own team and collaboratively. Qualifications Must-Have PhD with 2+ years of relevant experience Expertise in qPCR, digital PCR, DNA and RNA extraction, and experimental design
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Remain current in the scientific literature and state of the art techniques. Qualifications Must-Have Candidate should have a PhD in virology and/or immunology with at least 6+ years of relevant experience
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. What You Will Achieve Drug Safety Research & Development (DSRD) is
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to support decision making in the drug development process. The General Toxicology R6 Study Director is responsible for the design, conduct, interpretation, and reporting of exploratory, mechanistic and GLP in
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. ROLE SUMMARY As a member of our NGS and Data Science team, you will
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set-up. Proactively coordinate with Clinical Scientists and Lead Clinician to assure understanding and agreement on deliverables throughout the process Provide input for the design of the Statistical
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experiment design. These goals will be achieved through partnership with other disciplines including data scientists, analytical chemists, engineers, and process chemists to develop digital and robotic