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JOB SUMMARY With guidance, contribute to the development of the model informed drug development (MIDD) plans for an assigned project in order to optimize prospective studies, inform drug development
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. Contributes to medical review and interpretation of efficacy and safety data from clinical trials; this includes delivery of top-line report in collaboration with study statistician, and delivery of clinical
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committees, review opportunities for potential in-licensing, including performance of due diligence reviews, and aid new business development on market opportunities and the target product profile
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Job Details: Last Date to Apply for Job: 09 JULY 2024 Eligible for Employee Referral Bonus Work Location Assignment:On Premise On Premise colleagues work in a Pfizer site because it's needed to get
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conformance with Departmental requirements. Where applicable, performs job responsibilities in compliance with cGMP/GLP and all other regulatory agency requirements. Qualifications Must-Have Experience working