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quality of assigned laboratory projects in the Brussels PCRU in accordance with scientific, medical and ethical principles and with GxP requirement guidelines. Also accountable for training of data cache
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of program inspection readiness at all times. Establishing and maintaining engagement with Global Regulatory Affairs (GRA) Quality COE and Medical Quality Assurance (GCP quality) is critical. The role
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of program inspection readiness at all times. Establishing and maintaining engagement with Global Regulatory Affairs (GRA) Quality COE and Medical Quality Assurance (GCP quality) is critical. The role
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needs, engaging them in a flexible and constructive manner to address matters of ethical review with a focus on 3Rs, humane endpoints and adverse effects. Provide input to CM research projects in support
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ability to work independently or as part of a team, while demonstrating strong motivation with a dedicated work ethic with a commitment to timely delivery of high-quality work products while overcoming
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scientists to understand their research needs, engaging them in a flexible and constructive manner to address matters of ethical review with a focus on 3Rs, humane endpoints and adverse effects. Provide input
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of leadership, teamwork, ethical conduct, and adaptability in maintaining a robust compliance and quality culture within the team. Demonstrate resilience in the face of challenges, maintaining composure and
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needs, engaging them in a flexible and constructive manner to address matters of ethical review with a focus on 3Rs, humane endpoints and adverse effects. Provide input to CM research projects in support
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Activation Partner, CTRO and Local Regulatory, Medical Affairs colleagues and other key stakeholders as required) Ensures compliance to relevant Global and Local, internal and external requirements and
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scientific, medical, and ethical principles, within regulatory requirements/guidelines, and Pfizer SOPs Executes and is responsible for protocol required data and sample collection in accordance with ALCOA