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significant volume of projects developed in a field-based environment, while exhibiting the ability to prioritize, successfully implement, and demonstrate excellent judgment skills and work in a continuous
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transparent environment that encourages strong partnerships and mutual trust between teams, sub-teams, and therapeutics areas. Accountable to multiple project/core study teams and clinical sub-teams and manages
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, and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines. What You
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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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, the environment and product cost. This work will be performed in concert with multifunctional teams. A portion of your time will also be spent supporting existing active pharmaceutical manufacturing processes
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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