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The successful candidate will teach pathophysiology and pharmacology in the professional pharmacy curriculum to first, second, and third year PharmD students. Qualifications Applicants should have a PharmD, or equivalent degree, with preference of prior experience teaching in the professional curriculum of an ACPE accredited College of Pharmacy in the United States.
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G M.D., PhD, PharmD, DPH, EdD) or an advanced degree in Pharmacology, Pharmacy, Medicine, Nursing or equivalent experience is preferred; The Senior Medical Science Liaison (MSL) serves as a trusted scientific expert and partner representing Bayer in the medical community through the dissemination of and education on scientific data related to Bayer products across the product lifecycle.
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PhD, PharmD or equivalent in Pharmacokinetics, Pharmacology, Bioanalytical or related field with at least 5+ years of experience in Clinical Pharmacology, DMPK or related disciplines required.
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PhD or PharmD in pharmaceutical sciences, biomedical engineering, clinical pharmacology, or mathematical/statistical sciences with 5+ years of experience with clinical pharmacokinetic and pharmacokinetic- pharmacodynamic data analysis.
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Authors work orders when necessary QualificationsQualificationsMust be recognized applied development practitioner, experienced in both design and stewardship of clinical pharmacology components of clinical development plans and optimal application of pharmacometrics approaches to support decision making and regulatory successPhD or PharmD degree or equivalent degree with specialization in pharmacology or pharmacokinetics, or in a related scientific discipline.
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In order to be considered qualified for this role , you must have a PhD (eg, Pharmacometrics, Biology, Pharmacology, Engineering), PharmD, MD. We are looking for a highly motivated Principal Scientist, Clinical Pharmacology in our Pharmacometrics (PMx) group.
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QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.
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The school offers a BS in Pharmaceutical Sciences, MS in Pharmacology, PhD in Pharmacological Sciences, and Doctor of Pharmacy (PharmD.) As part of the Susan & Henry Samueli College of Health Sciences, we actively collaborate with schools and programs in medicine, nursing, and population, public health, and the Susan Samueli Integrative Health Institute to educate, train, and mentor the next generation of pharmaceutical scientists and clinical pharmacists.
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MD, or,PharmD with BCOP certification and significant hospital-based experience, or, PA with substantial clinical oncology experience, or DO. Oversee the evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies medicines in prostate cancer.
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PhD or PharmD degree or equivalent degree with specialization in pharmacology or pharmacokinetics, or in a related scientific discipline. MS in Pharmaceutical Science with job related experience in the field of drug development and clinical pharmacology.
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Masters or PharmD, with at least six years of experience, where "experience" means having a record of increasing responsibility and independence in a similar role in pharmaceutical drug development.
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We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.
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A clinical degree (e.g., RPh/PharmD, BSN, RN) Two years clinical experience in a medical setting, demonstrate general medical and pharmacology knowledge. A clinical degree (e.g., RPh/PharmD, BSN, RN.
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Medical resource for design and interpretation of clinical and preclinical programs to support existing and new development. Has a global perspective and mindset, with the ability to work effectively with colleagues from myriad.
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Work closely with other functional areas within R&D (clinical operations, data management, biostatistics, clinical pharmacology, nonclinical) to facilitate the execution of clinical trials and ensure high standards of study conduct are met.
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