- University of Miami (Miami, FL)
- …of Neurology has an exciting opportunity for a Full-time or Part-time statistical programmer to join an active clinical and translational research group focused ... ALS) in Miami, FL. Core Job Summary The statistical programmer will be an integral member of the research...checks to ensure data integrity and completeness + Write SAS macros and programs for data cleaning, reporting (eg… more
- Merck (North Wales, PA)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS /R programming experience in a clinical trial environment + MS in ... **Job Description** **Position Description:** **Associate Principal Statistical Programmer - Oncology (Hybrid)** In BARDS (Biostatistics and...Engineering or related field plus 7 or more years SAS /R programming experience in a clinical trial… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- …compliant SDTM and ADaM domains. Code is to be written using SAS , SAS procedures, or standardized macros. The Principal Programmer will assume a leadership ... As a Principal Statistical Programmer you will be a key member of the Clinical Development Operations, Statistical Programming Team. You will program routine and… more
- IQVIA (Nashville, TN)
- …complex project or client requirements. **Job Details:** + Position: - Principal Statistical Programmer + Home Based + Min 4+ years of CRO/Pharma Industry + ... Must have expertise of R programming as well as SAS (R) Base, and good knowledge of SAS (R)...+ Excellent application development skills. + Strong understanding of clinical trial data and extremely hands on in data… more
- Catalyst Clinical Research LLC (Wilmington, NC)
- …related field of study. Two (2) years related experience as a Statistical Programmer , SAS Developer Associate or any related position requiring statistical ... of study plus four (4) years related experience as a Statistical Programmer , SAS Developer Associate or any related position requiring statistical programming as… more
- IQVIA (Durham, NC)
- …set up by client **Education and Experience:** + Minimum 8 years' SAS programming experience within Clinical Research Organization or sponsor environment ... E9). + In addition to performing all senior statistical programmer duties, the Principal Statistical Programmer will...Serve as subject matter expert on all aspects of SAS programming + Understand pharmaceutical industry standards and trends… more
- Merck (Rahway, NJ)
- …statistical analysis and high-quality data to support decision making in clinical trials. The Associate Principal Scientist, Statistical Programmer supports ... Engineering or related field plus 9 or more years of SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs for ... clinical projects and may function as the Lead Clinical Data Programmer on multiple projects simultaneously....review listings and reports to support Data Management and clinical teams. Develop, implement and maintain SAS … more
- AbbVie (North Chicago, IL)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Statistical Programmer is an integral project team member in the research and development ... The primary responsibilities for this role include the analysis and reporting of clinical trial data under the direction and oversight of a Senior Statistical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …executes the programming and project standard under minimal supervision of the lead programmer and manager to support ongoing clinical studies and requests for ... The Senior Statistical Programmer provides support to the lead programmer...be for you if you have:** + Proficiency in SAS programming skills in a clinical data… more
- Weill Cornell Medical College (New York, NY)
- Title: Programmer Analyst II Location: Upper East Side Org Unit: Health Policy and Economics Work Days: Monday-Friday Weekly Hours: 35.00 Exemption Status: Exempt ... claims data, preferably Medicare data specifically, and coding expertise in SAS . **Job Responsibilities** + Queries large databases (millions of records) using… more
- IQVIA (Durham, NC)
- …requires strong SAS programming skills and industry experience working with clinical trial data._ IQVIA is hiring to expand a data visualization team, offering ... Follow steps to set-up studies and generate visualizations through Spotfire. + Preprocessing clinical data using SAS . + Producing data visualizations using … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …**This role may be for you if have:** + Good SAS programming skills ( SAS (Base, Stat, Macro, graph) in a clinical data environment + Good understanding of ... A senior pharmacometrics programmer provides timely support to the study team...matters according to the project strategies. Processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, … more
- Actalent (Raleigh, NC)
- Top Skills' Details The Statistical Programmer is responsible for supporting the Biostatistics and Statistical Programming team in delivering high-quality SAS ... programming services. Key duties include the development and review of SAS programs and outputs to effectively manage and report clinical trial data. This role… more
- ThermoFisher Scientific (Greenville, NC)
- …employment selection decisions.** **Knowledge, Skills and Abilities:** + Proven experience as a programmer in a clinical trial setting. + Strong knowledge of ... **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** **Trial Programmer Specialist III** Are you ready to join a team that… more
- Sanofi Group (Swiftwater, PA)
- **Statistical Programmer - VIE Contract** + _Location:_ _US, Swiftwater_ + _Target start date: 01/02/2025_ iMove, the Sanofi VIE Program, is available to citizens of ... submission of our Vaccine trials. The Scientific Programming team primarily focuses on clinical trials, with some support to pre- clinical and non- clinical … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …authority requests. **This role may be for you if have:** + Proficiency in SAS programming skills in a clinical data environment with excellent analytical ... The Principal Statistical Programmer will lead and support all programming activities...independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission,… more
- Dana-Farber Cancer Institute (Boston, MA)
- The Senior Data Programmer Analyst under the Associate Director, Data Analysis and Management, will be key to the completion of outcomes and translational research ... works closely with investigators, directors, program and project managers, clinical research coordinators, research data specialists, computational biologists and… more
- IQVIA (Miami, FL)
- …areas. We are seeking a highly skilled and motivated Principal Statistical Programmer with expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to join our ... dynamic FSP team. Position Overview: As a Principal Statistical Programmer with a specialized focus on PK/PD, you will...pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising… more
- Merck (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field and at least 5 years SAS programming experience in a clinical trial environment or + MS in ... Engineering or related field and at least 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment. **Required Skills:** + Effective interpersonal skills… more