- GRAIL (Menlo Park, CA)
- …and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome ... and healthcare companies. For more information, please visit grail.com The Senior Clinical Data Manager (CDM) will lead data management activities for one or… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Director, Data Management and Systems collaborating closely with MCA - Medical Affairs and Clinical Affairs - as well as Health Economics and Market Access (HEMA) to ... run biostatistics and data management in support of clinical evidence generation strategies across the Gastrointestinal Solutions (GIS) / Surgical & Interventional… more
- Parexel (Columbia, SC)
- …for overseeing centralized monitoring activities for global and/or complex clinical trials, ensuring the effective configuration, execution, and maintenance of ... trends, and issues. Proficiency in programming languages such as R, SQL, or SAS will be essential for creating custom analyses, automating workflows, and integrating… more
- Parexel (Indianapolis, IN)
- …analytics and statistical software/tools** such as **WinBUGS, R, Stata, Python, and SAS ** is required. **Key Accountabilities** + Provide expert input on the design ... of clinical development programs to ensure Access/HTA evidence needs are.... + Proficient in **R** and **GitLab** (experience with SAS , Python, WinBUGS, JAGS, or other relevant statistical software… more
- GAP Solutions Inc (Atlanta, GA)
- …questionnaires, and data collection instruments. + Conduct epidemiologic analyses using SAS , R, or equivalent; write/troubleshoot code. + Clean data; build reports; ... + **Ability to analyze and report on complex datasets using statistical software (eg, SAS or R)** + **Ability to work effectively with CDC staff across multiple… more
- TechData Service Company LLC (San Francisco, CA)
- …develop statistical analysis plan Assist in writing relevant sections of the clinical study report and publication Monitor internal and CRO project activities ... including timelines, deliverables and resources Ability to use SAS or R to perform efficacy analyses and validate important data derivations when necessary. Develop… more
- Cordis (Irvine, CA)
- …oversight of statistical design, analysis, and reporting across SELUTION DEB clinical programs. This role ensures the scientific integrity of all biostatistical ... methods, and leads internal and external data management partners to support clinical development and regulatory submissions. **Key Responsibilities** + Serve as the… more
- CSL Behring (King Of Prussia, PA)
- …(AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical ... methodologies applied to study design and data analysis for clinical trials and regulatory submissions + Influence and contribute...and written in English) + Good working knowledge of SAS and/or R + Expertise in a range of… more
- CSL Behring (King Of Prussia, PA)
- …and strategic partnering with key stakeholders for life-cycle-management (LCM) clinical trials initiated by the commercial organization; evaluate alternatives to ... traditional randomized clinical trials that make use of electronic health records,...A solutions oriented mindset + Hands-on programming skills in SAS / R **Working Conditions** + This is a… more
- Parexel (Sacramento, CA)
- …work remotely. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will ... randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents + Perform sample-size… more
