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Assist in regulatory affairs by supporting more experienced personnel. Responsibilities include reviewing labeling for products, drafting correspondence, managing project responsibilities, and preparing documents for FDA meetings and submissions. Maintain knowledge of current regulations and guidelines while providing technical assistance and proactive support during project management.
The Senior Clinical Pharmacology Specialist will lead the clinical pharmacology strategy for phases 1-4 in Clinical Development, develop dosage and administration strategies, and ensure the scientific quality of relevant documents. This role is cross-functional, involving collaboration with various teams and some travel.
The Administrative Specialist will perform diverse administrative tasks, coordinate processes, develop reports and presentations, manage calendars, support project teams, and oversee various office duties, including budget tracking and correspondence management. They will interact with upper management and guide lower-level administrative staff.
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The Senior Specialist - EEO Investigations will assist EEO investigators in addressing internal and external complaints, conduct EEO investigations, perform data analysis, develop action plans, and ensure case management accuracy. The role involves collaboration with various departments to facilitate effective investigations into EEO-related matters.
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