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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. POSITION SUMMARY As a Senior Scientist in the Molecular
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for scientific meetings and advisory boards Conduct literature reviews and prepare summaries to support clinical development programs Medical resource for design and interpretation of clinical and preclinical
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for designing the right media data for MROI effectiveness maximization. They will be a data driven and insight rich expert with expertise in the latest Martech tools and 1P & 3P data sources. RESPONSIBILITIES
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2, pre-submission meeting(s). Understanding of clinical trial design and management, including data flow process. Experience working in a highly matrixed, global and multi-site environment. Track
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Products (MDCP) Quality Operations team within the Pfizer Global Supply (PGS) organization. The incumbent provides quality assurance leadership/guidance of MDCPs related to design controls (21 CFR 820
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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. POSITION SUMMARY Pfizer's Oncology Research Unit (ORU) in La Jolla
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for stakeholders and asset teams for asset and study quality risk management, quality issues management and general GCP guidance. ROLE RESPONSIBILITIES Level 1 GCP Quality : IQMP (Integrated Quality Management Plan
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provides clinical pharmacology expertise to the project team including plan, design and oversee clinical pharmacology studies with operational assistance from operations colleagues Responsible for non
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ROLE SUMMARY The Global & US Medical Content Lead will plan and deliver an end-to-end medical channel content strategy across Pfizer medicines and therapeutic areas to optimize the engagement and
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ROLE SUMMARY The Global & US Medical Content Lead will plan and deliver an end-to-end medical channel content strategy across Pfizer medicines and therapeutic areas to optimize the engagement and