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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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notifying instrument key operators of upcoming reagent/supply needs. Process samples for analysis or storage. Utilize PIMS/LIS computer system for the processing of samples. Collect biological samples from
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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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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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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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resources to ensure all functional device activities are completed on schedule following the Pfizer Design Control process. Utilize technical writing and statistical data analysis skills to write protocols
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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