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processes, and implementing new technologies. Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and
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company and team with a desire to bring new, cutting-edge medicines to patients around the world. As a member of our team, you'll use science and technology to design, characterize and develop the solid
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consulting others. Serve as an SME. Train analysts on assays, provide mentorship and technical guidelines. Independently plan and prioritize their own workload to ensure timelines are met. Collaborate with and
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systems with the expectation that they can provide immediate assistance, education, and training for colleagues, contractors, and visitors on an as needed basis. With your deep knowledge in the discipline
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diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop, and coach others, oversee, and guide the work of other colleagues to achieve
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public pharmaceutical data sources to develop and inform financial modeling decisions Partner with key internal stakeholders to develop financial analysis supporting optimal financial investment in payer
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reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g., QRD, PLR
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RESPONSIBILITIES Evaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment Design and develop fit
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, in conjunction with country intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks. Site Care Partner Level 2 may be
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into QMS, share learnings across assets and across Oncology Quality team. Provide feedback to IQMP BPO to continuously improve IQMP approach. Develop and present quality point of view at governance meetings