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for the project teams to facilitate the IND submission operational process. Ensure direct report(s) in your group timely complete regulatory submission documents at the expected quality level. Proactively
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assets or CD&O process area and drive learnings across their tumor type(s). Lead Level 1 quality review/assessment during Due Diligence and/or Integration activities. Oversee program and study-level
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groups as required PHYSICAL/MENTAL REQUIREMENTS Sitting, ability to perform complex data analyses Work Location Assignment:On Premise The annual base salary for this position ranges from $99,900.00
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requires understanding of GCP and GMP to support the regulatory requirements and needs of different study types, quality management, inspection readiness, audit/inspection process, clinical trial processes
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of new risks and evolving existing risks in relevant Quality Risk Management (QRM) tools. Provide feedback to QRM Business Process Owner (BPO) to continuously improve Integrated Quality Management Plan
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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 As a Senior Associate Scientist, you will be
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Experience with laboratory automation, including Hamilton or open-source pipetting robots Experience with next generation sequencing and dataset analysis including alignments and variant detection PHYSICAL
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colleagues. Ensures that all regulatory development process commitments are clearly communicated, monitored and met. Acts as the point of contact for all internal Pfizer communication regarding the status
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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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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 As an Associate Scientist, you will be