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, external alliances or committees, consortia and academic relationships. BASIC QUALIFICATIONS PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, or PharmD
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experimental records within electronic laboratory notebook. Qualifications Must-Have BA/BS (5 years of experience), MS (2-4 years of experience) or, PhD (0-1 year of experience) in biology, immunology
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) and 13+ years of experience in the biopharmaceutical industry OR PhD/PharmD and 10+ years of regulatory submission experience in the biopharma industry. 5+ years of people management experience
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presentation of data at internal and external meetings. Qualifications Must-Have Doctorate degree PhD in Immunology OR Master's degree and 5 years of scientific/technical experience Track record of scientific
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resolution, best practices and opportunities for improving activities and relationships. BASIC QUALIFICATIONS PhD in toxicology, pharmacology, or other appropriate discipline with 8 years relevant professional
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Sciences with 7-10 years relevant experience or PhD Biological Sciences with 3-5 years of experience in relevant specialty area Advanced knowledge of physiological and pharmacological principles
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continuous improvement environment Maintain an up-to-date status for internal training requirements BASIC QUALIFICATIONS Bachelor's degree in a health science required PharmD, PhD, or equivalent terminal
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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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degree is preferred. In general, candidates for this job would have the following levels of experience: Bachelors - 15+ years or equivalent MS/MBA - 13+ years or equivalent PhD/PharmD/MD - 10+ years
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submission query response. Qualifications Must-Have MS in Chemical Engineering with 5+ years of experience or PhD in Chemical Engineering with 0-3 years of relevant experience Excellent knowledge of chemistry