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documents such as Pre-INDs, INDs, BLAs, and IMPDs. Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting
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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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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
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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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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