- Merck & Co. (Rahway, NJ)
- …global PK modeling and simulation stakeholders spanning all therapeutic areas. The senior programmer will gather and interpret user requirements, retrieve the ... and figures according to the modeling analysis plans. The programmer will take on a data stewardship leadership role...Life Sciences, Engineering or related field plus 5-9 years SAS programming experience in a clinical trial… more
- University of Southern California (Los Angeles, CA)
- Senior SAS Research Programmer - USC Schaeffer CenterApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA University-Park-Campus/ ... health behavior research and related health policy topics. The Senior SAS Research Programmer will...uniquely spans the entire spectrum of pharmaceutical development and clinical care - from drug discovery to regulatory approaches… more
- J&J Family of Companies (Irvine, CA)
- …and generation of analysis datasets, tables, listings, and graphs from assigned clinical sources using SAS and/or R; leading development and maintenance ... Learn more at https://www.jnj.com/medtech We are currently recruiting for a Sr Statistical Programmer to join our team based in Irvine, CA. This role can be… more
- J&J Family of Companies (Irvine, CA)
- …States of America **Job Description:** **Employer:** Biosense Webster, Inc. **Job Title:** Senior Programmer **Job Code:** A011.6006 **Job Location:** Irvine, CA ... of standard metric reports. Design, implement, and maintain the SAS programming algorithm for the clinical study...of experience in the job offered or in a Senior Programmer -related occupation. Alternatively, employer will accept… more
- Regeneron Pharmaceuticals (Warren, NJ)
- JOB RESPONSIBILITIES: * Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models ... timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and...in the biotechnology, pharmaceutical or health related industry. * SAS Certification desirable. EXPERIENCE: * 3 - 5 Year… more
- AbbVie (Florham Park, NJ)
- …products. + Analyze & report clinical trial data under direction of Senior Statistical Analyst. + Provide SAS programming support for clinical ... of work experience in each of the following: + providing SAS programming support for pharmaceutical industry clinical trials; + coding SAS programs using … more
- Regeneron Pharmaceuticals (Warren, NJ)
- A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a ... provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis… more
- Ascendis Pharma (Palo Alto, CA)
- …at least 7 years of relevant experience. + Proven experience as a lead programmer for clinical trials and complex technical projects. + Excellent knowledge of ... for employees to grow and develop their skills. The Senior Manager, Statistical Programming, will be expected to provide...expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This… more
- BeOne Medicines (San Mateo, CA)
- …industries or academic research. Experience with oncology trials. + Expert level SAS programmer with experience in delivering complex programming assignments and ... **Position Summary:** The Senior Manager, Statistical Programming is responsible for the...or equivalent related experience **Experience:** + Minimum 7+ years' clinical research and development programming experience using SAS… more
- Geisinger (Danville, PA)
- …needed to provide statistical support to clinical investigators. + Experienced SAS or R programmer for both data manipulation and statistical analysis. ... doctorate-level biostatistician. Responsibilities include collaborating on the design of clinical research studies, writing biostatistical analysis plans for research… more
- Teva Pharmaceuticals (West Chester, PA)
- …+ A minimum of 8 years of professional experience in a pharmaceutical or clinical research setting as a programmer including supporting regulatory submissions is ... required. + Hands-on expertise with R (Shiny, ggplot2), Python, Tableau/Spotfire and SAS is required. + Strong understanding of Clinical Trail data standards… more
- IQVIA (Durham, NC)
- **Job Level:** Senior /Principal Pharmacometrician, FSP **Location:** Home-based in the US or Canada **Why DSSS?** Data Sciences Staffing Solutions, DSSS or DS3, is a ... to development of protocols, analysis plans, PK/PD analysis, and pharmacometric reports for pre- clinical or Phase I-IV clinical studies. + Consult with … more
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