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Scientific programming in R, reproducible report writing via paradigm of statistically literate programming, creation of R packages, proficient technical writing, statistical analysis and modeling (e.g. regression analysis, time series analysis, computational statistics.
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Preprocessing clinical data using SAS.Programs visualization analysis datasets using SAS, R/R Shiny. Collaboration with staff in Biostatistics, Clinical Data Management, and Clinical Research and Global Drug Safety.
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Professional programming skills with SAS. SQL and R programming experience. Professional programming skills with SAS and SQL. R and/or Python programming experience is plus.
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At least 3 years of experience in statistical programming in SAS or R, and database programming in SQL or Python, demonstrated proficiency in statistical analysis programs commonly used in life sciences.
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Compliance with company and local IACUC/AAALAC regulations for animal research. Data collection including subcutaneous tumor measurements (caliper), body weight measurement, and clinical/animal health observations.
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Identify and support grant applications for Radiology Research; collaborate with the Clinical Research Office (CRO) and Program Managers in CRO in all grant administration. Work closely with the division of statistics and analytics in the Dept. of Clinical Research and Public Health.
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The Center for Translational Health Research and Interventions advancing Equity for Sexual and Gender Minorities (THRIVE) is housed within ISGMH. The THRIVE Recruitment and Retention (R&R) Core is made up of study staff involved in recruitment and retention activities.
$61,242 - $86,121 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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3-5 years of professional experience programming statistical analyses in SPSS, Stata, Python or R (Python and R highly preferred) We are seeking a Senior Research Analyst to help develop MLTs insights on advancing racial equity and socioeconomic mobility.
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Collaborates with the RD, RVP, CCO and Medical Lead to develop and implement new programming that is in line with evidence-based research and enhances Kolmacs current clinical and medical approach to care.
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In collaboration with project engagement leads, the candidate will provide clinical and statistical programming expertise to health economics and outcomes research studies to support pharmaceutical, biotech, and device technologies.
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Ph. D. in biostatistics or related discipline with 7+ years of experience with patient-reported outcomes, health economics, health technology assessment, and outcomes research methodology used in clinical trials and observational studies.
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Candidates must have experience with SAS, STATA, and/or R programming software. We aim to reduce social disparities in infection, chronic disease, and mental health by conducting integrative research across areas such as epidemiology, gerontology, sociology, infectious diseases, immunology, and laboratory research.
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Clinical Research Coordinator II - Onsite Onsite in Tustin Ca. and Redlands Ca. Why work at Tilda? As a Clinical Research Coordinator II with us, you will play a vital role in the advancement of medical science and the development of groundbreaking treatments.
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Licenses and Certifications Preferred: Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC.
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Licensures and Certifications: California Clinical Laboratory Scientist (CLS) License required. Two years of experience working as a clinical laboratory scientist (CLS) in a medical laboratory preferred.
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clinical research r programming jobs Company: J J Family Of Companies
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