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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 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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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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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 Designing new medicines at Pfizer
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development programs Medical resource for design and interpretation of clinical and preclinical programs to support existing and new development candidates Leads the preparations of the clinical content
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protocol design in collaboration with relevant Medical Affairs colleagues, and with input from external clinical experts as required Maintain a thorough knowledge of assigned protocols Conduct study start up
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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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discussions in assigned documents. Contributes to decision making about data presentation strategies to support advance planning of documents. Engages early with project teams and subject matter experts to plan
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Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits
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for this position ranges from $78,000.00 to $130,000.00.* In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 10.0% of the base salary. We