| Clinical SAS|R Programmer(Urgent Requirement) at Remote, Remote, USA |
| Email: [email protected] |
| From: ranjeet kumar, Source Infotech Inc [email protected] Reply to: [email protected] Hi, Role: Clinical SAS/R Programmer Location: Remote but must be in EST/CST Visa: No H1B,CPT,OPT Duration : 1 Year MOI: Video Minimum of 10 years of experience working for large pharmas/CROs We are seeking a highly skilled Clinical SAS Programmer with strong R programming experience to join our dynamic team. This role will involve working with clinical trial data, performing statistical analysis, and generating comprehensive reports to support clinical research and regulatory submissions. **Key Responsibilities:** 1. **Data Management:** - Develop and maintain SAS programs to import, clean, and validate clinical trial data. - Use R for data manipulation, analysis, and visualization. 2. **Statistical Analysis:** - Perform statistical analyses in accordance with study protocols and analysis plans. - Generate tables, listings, and figures (TLFs) using SAS and R. 3. **Report Generation:** - Create and QC statistical outputs and clinical study reports for regulatory submissions. - Document programming activities and ensure compliance with Standard Operating Procedures (SOPs). 4. **Collaboration:** - Work closely with biostatisticians, data managers, and clinical researchers. - Provide programming support for ad-hoc analysis requests and exploratory data analyses. 5. **Quality Assurance:** - Perform rigorous quality checks on all deliverables. - Maintain annotated datasets and ensure traceability of data processing. **Qualifications:** - **Education:** Bachelors or Masters degree in Statistics, Computer Science, Biostatistics, or a related field. - **Experience:** Minimum of 3 years of clinical SAS programming experience, with a strong background in R. - **Technical Skills:** - Proficiency in SAS and R, including data step programming, PROC SQL, and R packages for data analysis. - Experience with CDISC standards (SDTM, ADaM). - Knowledge of clinical trial processes and regulatory requirements (e.g., FDA, EMA). - **Soft Skills:** - Strong analytical and problem-solving skills. - Excellent communication skills, both written and verbal. I would appreciate your valuable reply. Have a nice day. Thanks and regards Ranjeet kumar , IT-Technical Recruiter Source Infotech Inc P.O. Box 577, EDISON, NJ 08818-0577 Web:www.sourceinfotech Id: [email protected] Keywords: active directory rlang information technology Idaho New Jersey Clinical SAS|R Programmer(Urgent Requirement) [email protected] |
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| Fri Sep 20 03:03:00 UTC 2024 |