- Merck & Co. (North Wales, PA)
- …Life Sciences, Engineering or related field plus 9 or more years of SAS programming experience in a clinical trial environmentMS in Computer Science, ... or related field plus 7 or more years of SAS programming experience in a clinical trial...years of SAS programming experience in a clinical trial environmentDepartment Required Skills and Experience:Excellent interpersonal skills… more
- Merck & Co. (Rahway, NJ)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS /R programming experience in a clinical trial environmentMS in Computer ... Engineering or related field plus 7 or more years SAS /R programming experience in a clinical trial...more years SAS /R programming experience in a clinical trial environmentRequired Experience and Skills: Excellent interpersonal skills… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to support drug development processes and global submissions as required for clinical trials. These include developing and validating SAS programs for ... provide complex data review listings and reports to support Data Management and clinical teams. Develop, implement and maintain SAS programming standards and… more
- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent… more
- Merck & Co. (North Wales, PA)
- …related occupation.Must have 3 years of experience with all of the following: SAS programming in a clinical trial environment including data steps, procedures, ... of potential medical breakthroughs.Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and... SAS /MACRO, and SAS /GRAPH; developing analysis and reporting deliverables for R&D projects… more
- Merck & Co. (Rahway, NJ)
- …drug/vaccine projects in Late Development Statistics.Lead the interaction with Clinical , Regulatory, Statistical Programming, Data Management, and our company's ... Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine… more
- Merck & Co. (North Wales, PA)
- …for related drug/vaccine projects in Late Development Statistics.Interacts with Clinical , Regulatory, Statistical Programming, Data Management, and other company ... Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.… more
- Genmab (Plainsboro, NJ)
- …leading a small team to complete various programming efforts within a clinical trial.You will be responsible for ensuring integrity, consistency, and adherence to ... to the Director, Programming, and work closely with Data Management, Clinical Programming, Statistics, Medical Writing, and other functions as necessary.Position… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to understand the drug development, learn about statistical applications in clinical trials, and explore/establish their interests in pharmaceutical industry for ... member; Sufficient skills in at least one of the two programming languages: SAS or R; Good communication skillsQualified candidates must currently be enrolled in an… more
- AAOS (Des Plaines, IL)
- …join a team of like-minded colleagues who share your vision of advancing clinical practice through rigorous research and analysis. You take pride in delivering ... reliable and relevant information to inform clinical decisions. You are eager to dive into the...reviews. Experienced in the use of STATA, SPSS, or SAS statistical software packages. Familiarity with evidence-based medicine processes,… 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 ... Engineering or related field plus 7 or more years SAS /R programming experience in a clinical trial...more years SAS /R programming experience in a clinical trial environment **Required Experience and Skills:** + Excellent… more
- Merck (Rahway, NJ)
- …Mathematics, Life Sciences, Engineering or related field plus 9 or more years of SAS programming experience in a clinical trial environment + MS in Computer ... or related field plus 7 or more years of SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** + Excellent… more
- Pfizer (Collegeville, PA)
- …**Must-Have** + Bachelor's Degree + 7+ years' experience + 5+ years' experience with SAS programming in clinical setting + Demonstrated relevant experience in a ... discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and...is our mission to strengthen the oversight of our clinical data through stronger ownership, control, and visibility. You… more
- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. MS in ... Engineering or related field plus 7 or more years SAS programming experience in a clinical trial...more years SAS programming experience in a clinical trial environment. **Department Required Skills and Experience:** +… more
- Taiho Oncology (Princeton, NJ)
- …the integrity of statistical outputs. Performance Objectives: + Effectively designs/develops SAS programs for clinical study reports, for regulatory submission, ... project status and provides ongoing risk assessments. + Responsible for maintaining/archiving clinical database, SAS programs and results, and documentations. +… 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 ... review listings and reports to support Data Management and clinical teams. Develop, implement and maintain SAS ...and clinical teams. Develop, implement and maintain SAS programming standards and performs quality checks. + Review… more
- IQVIA (Durham, NC)
- …set up by client **Education and Experience:** + Minimum 8 years' SAS programming experience within Clinical Research Organization or sponsor environment ... specifications + Serve as subject matter expert on all aspects of SAS programming + Understand pharmaceutical industry standards and trends and proactively plan,… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …equivalent in a closely related field is preferred + Minimum of 8 years clinical SAS programming experience in the pharmaceutical industry + Experience with ... (edaravone) oral suspension in 2022. The company handles research, clinical development, sales, marketing, medical affairs, supply chain,and business development… more
- Banner Health (AZ)
- …required. Strong technical skills as appropriate for position (SQL/Ansi SQL, SAS , Tableau, Excel, clinical software applications, etc.). PREFERRED QUALIFICATIONS ... **Primary City/State:** Arizona, Arizona **Department Name:** IT Clinical Care-Corp **Work Shift:** Day **Job Category:** Information Technology You have a place in… more
- Banner Health (Phoenix, AZ)
- …required. Strong technical skills as appropriate for position (SQL/Ansi SQL, SAS , Tableau, Excel, clinical software applications, etc.). PREFERRED QUALIFICATIONS ... **Primary City/State:** Phoenix, Arizona **Department Name:** Clinical Performance Analytics **Work Shift:** Day **Job Category:** Information Technology Good health… more
