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bio-functional assays, including information/data archiving, Standard Operating Procedure and status reports. Assist in ordering supplies from internal inventory and prepare reagents/supplies necessary
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bodies, and other internal and external stakeholders. In close partnership with medically qualified colleague/s, analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues
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multidisciplinary team environment. Ensure appropriate use of animals in compliance with all regulatory requirements and internal standards. QUALIFICATIONS Must-Have Bachelor's degree with 6+ years relevant
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. Responsibilities include de novo antibody initiation, oversight of CROs, internal interface with stakeholders. Perform reagent modifications, characterization, and immunogen preparation. The candidate will be
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of best practices and process improvements with the vendor. The role may require some coaching of internal colleagues in working with vendors and the identification of areas where targeted training
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, and present data internally to cross functional teams. - Prepare and present project summaries at team meetings, departmental meetings, and through summary reports. Contribute to the preparation
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internal policies. Facilitate and lead the development and execution of ancillary in vitro assays necessary to maximize value of the contribution by the in vivo team, if necessary. Interpretation
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and pharmacokinetics to drive drug discovery and development programs across Pfizer's therapeutic areas including oncology, internal medicine, inflammation and immunology, and rare diseases. Working
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in the marketplace. Is dedicated to meeting the expectations and requirements of internal and external customer's; always focused on patient safety first, establishes and maintains effective
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ROLE SUMMARY Our Internal Medicine (IM) Medicinal Chemistry Group delivers scientific excellence in the small-molecule medicinal chemistry portfolio aligned to the IM Research Unit (IM RU). You will