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intelligence to aid in experiment design. These goals will be achieved through partnership with other disciplines including data scientists, analytical chemists, engineers, and process chemists to develop
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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may
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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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HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In collaboration with Global
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HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In collaboration with Global
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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 You will participate in pre-clinical oncology
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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 The Protein and Bioanalytical Sciences (PBS
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unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In
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unsolicited medical requests from HCPs in a manner that complies with all applicable Pfizer guidelines, policies, and procedures. Field relevant inbound queries from HCPs via established triage process. In