- Merck & Co. (North Wales, PA)
- …:Address operational challenges that require strategic solutions, resulting in improved Clinical Study Report and filing completion timelines worldwide. Lead ... of internal stakeholder groups including the Outcomes Research and Clinical Safety organizations. Lead and actively contribute to...Life Sciences, Engineering or related field plus 12 years SAS programming experience in a clinical trial… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …utility development preferred- Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming preferred- Advanced ... build up standard on SDTM/ADaM datasets, and TFLs.Responsibilities- Supporting project lead on outsourced projects, act as statistical programming subject matter… 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
- General Dynamics Information Technology (Fort Detrick, MD)
- …Citizenship Required:** Yes **Job Description:** **GDIT's Military Health team is hiring a SAS programmer to support the Office of Regulated Activities (ORA) ... **Public Trust/Other Required:** NACI (T1) **Job Family:** Programming **Skills:** Datasets, SAS ,Statistical Programming **Experience:** 5 + years of related experience… more
- Adecco US, Inc. (Boston, MA)
- …to the Lead of Clinical Data Programming, Data Management, the clinical programmer works in varied therapeutic areas, develops and validates SAS /SQL ... a local client in their search to fill a Clinical Data Programmer in Boston, MA. Apply...Program listings, tables, profiles, figures, and standard datasets in SAS /SQL per the best practices, standard processes, and specifications… more
- ThermoFisher Scientific (Wilmington, NC)
- …projects in the Clinical Pharmacology department. Works independently in a lead programmer role on select moderately sophisticated studies, or may serve ... **Key responsibilities:** + Acts as the lead programmer or project lead on Clinical...and SOPs. + Independently creates, implements, maintains, and validates SAS programs that transfer data across multiple data management… more
- IQVIA (Austin, TX)
- …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
- Trinity Health (Livonia, MI)
- …Electronic Health Record (EHR) source systems, Epic preferred, and healthcare clinical workflows.** **POSITION PURPOSE** The Data Programmer Analyst (II) ... to collaboratively facilitate the transformation of data to knowledge. The Data Programmer Analyst (II) must demonstrate effective and strong communication with the… more
- IQVIA (Durham, NC)
- …a Global Pharma company. We are now expanding this team by adding a Principal/ Lead level Statistical Programmer . Expect to be dedicated to this sponsor, working ... expectations of you:** + 9 years or more in SAS programming for clinical trial data, working...+ 4 years or more working as a study lead for statistical programming activities. + Bachelor's degree in… 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
- Johns Hopkins University (Baltimore, MD)
- …infections and other health disparities through research, programmatic and clinical endeavors. The successful candidate will be responsible for supporting ... programming for projects with continued ongoing support. + Manage clinical and other types of data sets and conduct...Office + Familiarity with a statistical analysis program (STATA, SAS or R preferred) + Ability to communicate effectively… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Takeda Development Center Americas, Inc. is seeking a Manager, Statistical Programmer in Lexington, MA with the following requirements: Master's degree in ... of analysis datasets, dataset specifications, statistical tables, figures, and listings for clinical trials; create standard macros that can be adapted to multiple… more
- Merck (Rahway, NJ)
- …in support of internal stakeholder groups including the Outcomes Research and Clinical Safety organizations. + Lead and actively contribute to departmental ... Study Report and filing completion timelines worldwide. + Lead development of therapeutic areas- specific standard Tables, Listings,...Life Sciences, Engineering or related field plus 12 years SAS programming experience in a clinical trial… 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 ... for submissions + Project/Study lead experience strongly preferred + Education/Experience: Bachelor's Degree in...leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We… 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …utility development preferred - Advanced working knowledge of all aspects of the SAS programming language used in clinical trials programming preferred - ... standard on SDTM/ADaM datasets, and TFLs. **Responsibilities** - Supporting project lead on outsourced projects, act as statistical programming subject matter expert… more
- Amgen (Washington, DC)
- …required standards and are statistically accurate. The Biostatistical Programming Senior Manager (Product Lead Programmer ) lead a group of Oncology and other ... assigned staff at product level according to priorities. + Lead and/or participate in departmental process improvement initiatives and...industry experience **Preferred Qualifications:** + In depth knowledge of SAS Graph, SAS STAT, SAS … more
- Edwards Lifesciences (CA)
- …will make an impact:** + Develop, test, validate, document, maintain and execute programs in SAS and serve as lead programmer . He/she will take primary role ... expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of...in review and validation of SAS programs created by more junior-level programmers. In addition,… more
- IQVIA (Durham, NC)
- …macros or writes SAS (R) macros to automate study deliverables. + Works as a Lead Biostatistician or Lead Programmer for multiple Phase 1-4 studies. + ... activities and departmental initiatives. + Works with-in the Global Clinical Data Standards team in collaboration with each data...Assists in submissions of electronic data (eg, SAS (R) data sets) to regulatory agencies. + Independently develops… more
- Astellas Pharma (Northbrook, IL)
- …/ Medical Affairs Statistician (MA) / Exploratory Statistician / Regional Statistician Lead (RSTATL) or Lead Product Statistician (LPS) for routine works ... in an established area ( clinical / observational studies, MA tactic, Biomarker & PK/PD Analyses...is expected to understand when to seek Global Statistical Lead (GSTATL) and/or line management intervention to ensure successful… more
