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Key responsibilities for Associate Director of Biostatistics are: Driving the statistical strategy of the designated projects taking into consideration the impact across Development.
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Job Qualifications· Ph. D. in Computational Biology, Biostatistics, or a related field. The qualified candidate will report to the Head of Clinical Data Science and is expected to have the following responsibilities:· Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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We are seeking a highly skilled and experienced individual to join our team as an Associate Director of Oncology Genomics. Basic Qualifications:PhD in a quantitative subject e.g. Bioinformatics, Biostatistics, Computational Biology, Epidemiology with combined academic and or industry experience of 8+ years.
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Reporting to the Associate Director, Medical and Regulatory Writing, the Senior Manager, Regulatory Technical Writer will be a key member of the Clinical Development organization and interface with cell therapy clinical, nonclinical, and manufacturing research personnel in the production of high-quality documentation that is appropriate for its intended audience (e.g. regulators, tech transfer recipients, journal editors, NIH, clinical trial sites/investigators.
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Areas of priority include (1) medicinal chemistry, (2) biochemistry, (3) pharmacology, (4) physiology, (5) pharmacy, or (6) associated medical fields, such as biostatistics. Manages FWSOP and departmental research capabilities, such as lab equipment purchases, maintenance and inventory Leads creation and presentation of ad hoc reports to the Dean and FWSOP administration as neededFaculty member holding this title reports to the Dean for the responsibilities associated with this Director role and to department chair for other responsibilities;Work allocation for this role is 30-40% effort and is classified as service.
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The Associate Medical Director will serve as the Medical Lead for Vertex clinical trials in Cystic Fibrosis (CF), working with cross-functional multidisciplinary study teams on clinical trial strategy, design and execution and serving as the primary Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials.
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Oversees a diverse and highly skilled group of experts in clinical medicine, epidemiology, biostatistics, public policy, and data management and analysis, including Directors, Associate Directors and Technical Leads.
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The Associate Director, Clinical Development is part of the Development Physician team at Janssen Immunology, with clinical development and medical/scientific responsibility for Phase 2 and 3 programs, and providing applicable disease area expertise (including Gastroenterology for the Therapeutic Area (TA.
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The Associate Director / Director Biostatistics is a senior level statistician responsible for the supervision (Director level, in a matrix way) of other statisticians, provides statistical leadership and has a major influence on the technical capabilities of the department.
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The Department of Internal Medicine, Divisions of General Internal Medicine, Hospital Medicine, and Endocrinology are seeking a full-time Assistant/Associate Professor of Research to serve as the Director of Outcomes Research in their divisions.
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As the Associate Director, Biostatistics, a typical day might include the following:This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development.
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Master's degree in statistics or biostatistics with 8+ years of biopharmaceutical statistics experience with specific experience in late stage drug development, including phase IIb, phase III, and submissions in the pharmaceutical industry.
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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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PhD (6+ years' experience) or MS (8+ years' experience) in statistics or biostatistics or related scientific field with clinical trials, drug development, pharmaceutical industry or healthcare experience.
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The Associate Biostatistics Director acts as fully independent global statistical lead, representing Data Science in Core Teams (CMT or Development Core Team). PhD or M.S. in Biostatistics, Statistics or related scientific field.
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