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The Labeling Operations Manager (LOM) provides operational support for the initial creation and relevant updates to labeling documents including the Core Data Sheets (CDS), United States Package Inserts (USPI), Summary of Product Characteristics (SPC) for products registered in the EU via the...
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ROLE SUMMARY The Sr. Manager, Specialty Access Solutions is responsible for ensuring the quality and validity of data obtained from Pfizer contracted specialty pharmacies, in order that it be utilized with full confidence in a compliant manner, these include: insights generation, field...
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ROLE SUMMARY As a member of our Oncology team, you will play a critical role in supporting Translational Science Operations strategies, through scientific technical oversight and management of external and internal partners involved in the implementation of clinical trial biomarkers sample...
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The Study Operations Manager is responsible for study and regional/country level activities from study startup through conduct and study close. The Study Operations Manager will be assigned one or more studies and will be tasked with taking on several responsibilities in support of the larger...
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POSITION SUMMARY You will join a team of scientists supporting oncology development programs. You will be the primary Clinical Pharmacology Lead providing clinical pharmacology expertise to a multidisciplinary project team of an oncology program. KEY RESPONSIBILITIES Act as Clinical Pharmacology...
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The Labeling Operations Manager, Senior Associate provides operational support for the initial creation and relevant updates to labeling documents including the Core Data Sheets (CDS), United States Package Inserts (USPI), Summary of Product Characteristics (SPC) for products registered in the...
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ROLE SUMMARY The Medical Writer (Manager) creates documents pertaining to clinical studies and regulatory interactions, including (but not limited to) protocols, clinical study reports , briefing documents, clinical summaries for marketing applications, and responses to queries from regulatory...