- Merck & Co. (Rahway, NJ)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment.MS in Computer ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Effective… more
- Merck & Co. (North Wales, PA)
- …and simulation stakeholders spanning all of our company's 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 years SAS programming experience in a clinical trial… more
- DivIHN Integration Inc (Deerfield, IL)
- …regarding the following opportunity, please contact our Talent Specialists Meghna at ### Title: Clinical SAS Programmer Location: Deerfield, IL Duration: 12 ... Hybrid - 3 days onsite/ 2 remote - no preference on days. Description: Senior Statistician Responsible for clinical trial with clinical study methodology… more
- Piper Companies (Raleigh, NC)
- Piper Companies is looking for an experienced Principal/ Senior Statistical Programmer to join a well-established, global clinical research organization ... define.xml, SDRG/ADRG, etc.Qualifications of the Principal/ Senior Statistical Programmer :. 5+ years of experience with SAS ...Statistical Programmer :. 5+ years of experience with SAS programming with clinical trial data and… more
- Point32Health (Boston, MA)
- …improve health care delivery and population health through research and education and SAS Programmer /Analysts play a critical role in delivering on that mission. ... the most pressing health problems facing health plan delivery systems. Our SAS Programmer /Analyst team members are responsible for drafting and implementing… more
- Actalent (San Diego, CA)
- …evaluation of technical infrastructure to expedite conduct and evaluation of clinical trials and basic research. Performs statistical analysis and develops tracking ... systems to determine the efficiency of clinical trials. Evaluates databases and statistical analysis programs and...Plan (SAP) Write or modify efficient design and code SAS programs using BASE/ SAS , SAS /STAT,… more
- ICON Clinical Research (Blue Bell, PA)
- …that ensures what we do, we do well. We have an incredible opportunity for a ** Senior Statistical Programmer II** to join the diverse and dynamic team within the ... need:** + 8+ years of experience successfully performing the role of Statistical Programmer , in the clinical research industry + Experience with leading multiple… more
- IQVIA (Los Angeles, CA)
- …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)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years SAS programming experience in a clinical trial environment. + MS in ... Life Sciences, Engineering or related field plus 3 years SAS programming experience in a clinical trial...3 years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** +… more
- Novo Nordisk (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... Science, serving as a key contact point into the Clinical Data Science and Evidence (CDSE) Real World Evidence...Evidence (CDSE) Real World Evidence (RWE) team. Relationships The Senior Manager reports directly to a Senior … more
- IQVIA (Durham, NC)
- …over design, and supported pooling of PK parameters required + Strong SAS technical skills and in-depth CDISC knowledge + Good knowledge regulatory requirements ... IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing… more
- Merck (North Wales, PA)
- …and simulation stakeholders spanning all of our company's 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 years SAS programming experience in a clinical trial… more
- Abbott (Alameda, CA)
- …year in device or pharmaceutical clinical trials as a clinical programmer performing mentioned above functions using SAS , Oracle Clinical or ... Systems/IT mainly (data management secondly). Incumbent will be supporting Senior Manager to achieve metrics related to activities in...tables, listings, reports, and ad hoc queries from Oracle Clinical and related databases using SAS or… more
- Amgen (Washington, DC)
- …activities meet required standards and are statistically accurate. The Biostatistical Programming Senior Manager (Product Lead Programmer ) lead a group of ... a career you can be proud of. **Biostatistical Programming Senior Manager** **Live** **What you will do** Let's do...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
- Astellas Pharma (Northbrook, IL)
- …**Purpose and Scope:** Member of cross-functional teams, the primary purpose of the Senior Manager is to act independently as Study Statistician / Medical Affairs ... Lead Product Statistician (LPS) for routine works in an established area ( clinical / observational studies, MA tactic, Biomarker & PK/PD Analyses or local project).… more
- Ascendis Pharma (Palo Alto, CA)
- The Senior Manager, Statistical Programmer will be expected to provide timely support to the study team on all programming matters according to project ... specification and provide programming support for all of required deliverables. + Process clinical data required for statistical analysis. Develop SAS code or… more
- University of Colorado (Aurora, CO)
- …or research field. + 2 or more years of experience as a statistical programmer and/or statistician in clinical research with track record of collaborating on ... peer-reviewed publications and data analysis. **Minimum Qualifications Senior Research Associate:** + A Master's degree in (bio)...7 or more years of experience as a statistical programmer and/or statistician in clinical research with… more
- Ascendis Pharma (Palo Alto, CA)
- …providing oversight of Statistical Programming FTEs, contractors, and CROs. + Processing clinical data required for statistical analysis. Develop SAS code and ... programming activities to support drug development? Do you have experience within SAS and CDISC standards, project and resource management? If so, you have… 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
