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to achieve meaningful outcomes and create business impact. Advanced scientific/healthcare degree required (PharmD, PhD, MS, etc.) Minimum 6 years experience in the healthcare/pharmaceutical sector with 3
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degree, preferably in a life science discipline. BS/BA +5 years, MS/MA +3 years, PhD +0 year s of experience in medical writing or related field. Understanding of the role of each member of cross
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+ years of experience . MS, PharmD, PhD or MD preferred. Equivalent workplace experience can be considered. Extensive direct regulatory experience, preferably including as a Global Regulatory Lead and
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development to support launch and post-launch success. BASIC QUALIFICATIONS Clinically trained (MD, ClinPharm), PharmD, MD-PhD desired Oncology medical professional with strong experience (at least 9 years if
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PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, or PharmD Strong written and verbal communication skills PREFERRED QUALIFICATIONS Experience
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years or equivalent PhD/PharmD/MD - 9 years or equivalent Extensive knowledge of ICH GCP and regulations in order to assess GCP situations and coordinate resolution activities across partner lines. Expert
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compliance. Provide subject matter expertise and guidance to colleagues. Lead / co-lead complex pilot studies and projects across preclinical Pfizer Oncology enterprise. BASIC QUALIFICATIONS PhD with 4+ years
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discoveries in cancer research into the best medicines imaginable for patients. Pfizer's ORU in La Jolla, California, is seeking a Postdoctoral candidate (PhD) forthe Oncogene & Cancer Vulnerabilities (O&CV
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significant findings via internal and external presentations or publications MINIMUM QUALIFICATIONS Recent PhD with 1-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience
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and guide the work of other colleagues to achieve meaningful outcomes and create business impact. Advanced scientific/healthcare degree required (PharmD, PhD, MS, etc.) Minimum 6 years experience in