- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field plus 12 years SAS programming experience in a clinical trial environment.MS in Computer ... Mathematics, Life Sciences, Engineering or related field plus 10 or more years SAS programming experience in a clinical trial environment. Department Required… more
- Merck & Co. (North Wales, PA)
- …Applied Mathematics, Life Sciences, Engineering or related field and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer ... Engineering or related field and at least 3 years SAS programming experience in a clinical trial...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …Bachelor's degree plus minimum 9 years or Master's plus minimum 7 years SAS programming experience in a clinical trial environmentExperience leading large and/or ... Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple...and according to quality, compliance and timeliness requirements.-Expertise in SAS and clinical trial programming including data… more
- Harvard University (Cambridge, MA)
- …II Department Office Location:USA - MA - Boston Business Title: SAS Programmer ISub-Unit: Appointment End Date:30-Nov-2027Salary Grade ... Experience with data cleaning + Knowledge of statistical and/or clinical trials + Strong attention to detail, as well...+ assisting with the transition to CDISC system The SAS Programmer will perform other duties as… more
- WCG Clinical (Princeton, NJ)
- …required **QUALIFICATIONS/EXPERIENCE:** + At least five years of post-Bachelor's experience in Clinical SAS Programming, analyzing data, working in a team ... Principal Statistical Programmer ( Remote ) **General Information** **Location:** Princeton,...environment, and participating in managing projects. + Extensive SAS programming in a clinical trial setting… more
- Ascendis Pharma (Palo Alto, CA)
- …for employees to grow and develop their skills. The Clinical Data Programmer will be responsible for performing SAS programming ( SAS /SQL program ... clinical data review and process efficiency. The Clinical Programmer will lead clinical ...analytical skills using BASE/ SAS , SAS /STAT, SAS MACROS + Strong knowledge of Oncology clinical… more
- ICON Clinical Research (Blue Bell, PA)
- …will need:** + 3+ years of experience successfully performing the role of Statistical Programmer , in the clinical research industry + Experience with SDTM, ADAM, ... ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we...well. We have an incredible opportunity for a **Statistical Programmer II** to join the diverse and dynamic team… more
- Merck (Rahway, NJ)
- …Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 12 years SAS programming experience in a clinical trial environment. MS in ... Mathematics, Life Sciences, Engineering or related field plus 10 or more years SAS programming experience in a clinical trial environment. **Department Required… more
- Allucent (Cary, NC)
- …therapies to patients in need across the globe. We are looking for an R programmer to join our global Clinical Pharmacology Modeling and Simulation (CPMS) team ... at Allucent in either Europe or USA. As a Senior Programmer /Analyst you will lead data programming and visualization activities across projects within CPMS. You will… more
- ICON Clinical Research (Blue Bell, PA)
- …need:** + 8+ years of experience successfully performing the role of Statistical Programmer , in the clinical research industry + Experience with leading multiple ... ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we...We have an incredible opportunity for a **Senior Statistical Programmer II** to join the diverse and dynamic team… 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...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Amgen (Washington, DC)
- …this vital role you will ensure all statistical aspects pertaining to clinical activities meet required standards and are statistically accurate. The Biostatistical ... Programming Senior Manager (Product Lead Programmer ) lead a group of Oncology and other therapeutic...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
- Harvard University (Cambridge, MA)
- …Administrator providing oversight for advanced application design and planning, Core programmer training, and clinical data standardization, respectively + ... applying: 1) Resume, 2) Cover letter, 3) Sample of SAS code (solely created by the applicant - preferably...seven years of high-level statistical programming skills in a clinical data environment or research setting, preferably with … 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 ... 7 or more years of experience as a statistical programmer and/or statistician in clinical research with...fluency in a core language such as R or SAS and advanced programming capabilities (eg SAS … 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 ... to support drug development? Do you have experience within SAS and CDISC standards, project and resource management? If...of summary tables, data listings and graphs required for clinical trials, and CDISC datasets for regulatory submission. This… more
- Merck (North Wales, PA)
- …+ Bachelor's degree plus minimum 9 years or Master's plus minimum 7 years SAS programming experience in a clinical trial environment + Experience leading large ... **Job Description** The Associate Principal Programmer leads the statistical programming activities for multiple...to quality, compliance and timeliness requirements. + Expertise in SAS and clinical trial programming including data… more
- Allucent (Cary, NC)
- …helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need ... We are looking for a Sr. Biostatistician (SrBios) to join our A-team (hybrid*/ remote ). As a SrBiosat Allucent, you are responsible for supporting the statistical… more
- Allucent (Cary, NC)
- …helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need ... We are looking for a Principal Biostatistician (PrBios) to join our A-team (hybrid*/ remote ). As a PrBios at Allucent, you are responsible for supporting the… more
- Harvard University (Cambridge, MA)
- …+ 7+ years of related statistical experience, including with multi-center clinical trials, or equivalent collaborative statistical experience required + Experience ... with statistical software (such as SAS , Stata, etc.) required Additional Qualifications and Skills: The following job-specific skills and competencies are preferred:… more
- Bristol Myers Squibb (Trenton, NJ)
- …**Experience Requirements** + Minimum of 4 plus years Pharmaceutical/CRO experience as a SAS Programmer supporting clinical trials for regulatory submissions ... guidelines and appropriate metadata to reflect tabulation datasets + Oversee/ develop SAS programs to generate SDTM datasets + Create and/or validate eCRT package… more
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