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feedback and conflict constructively. Demonstrate ability to manage a significant volume of projects developed in a remote environment, while exhibiting the ability to prioritize, successfully implement, and
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changing needs of the regulatory environment Works with RQA colleagues on cross GxP audit plans as required Coaches colleagues - leads training for routine and non-routine site and process audits Advises
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and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate
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colleagues the flexibility and tools they need. The Primary Pharmacology Group offers a collegial and supportive environment for colleagues, with a culture encouraging openness, innovation, and ownership
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. Knowledge of a pharmaceutical clinical research unit environment. Working knowledge of GxP, GCP, CAP and CLIA regulations. Demonstrates teamwork by effective participation in multifunctional teams, motivate
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simultaneous projects in a deadline-oriented environment Direct external vendors and manage budgets, timelines, and quality of deliverables PREFERRED QUALIFICATIONS Experience in assigned therapeutic area NON
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and key external stakeholders through strong interpersonal skills Strong organizational skills to track numerous tasks for multiple simultaneous projects in a deadline-oriented environment Direct
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, serum), detect the presence of anti-drug antibody and neutralizing anti-product antibody activity utilizing various platform in a regulated (GLP, GCP) environment against challenging timelines. Timely
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performing culture of innovation, impact, trust, accountability, and mutual respect in a fast-paced matrix environment Demonstrate our values and behaviors of Excellence, Courage, Equity and Joy. Exemplify
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of the discipline will make you a critical member of the team. You are proactive in contributing to all team discussions and creating an environment of collaboration. It is your hard work and focus that will help in