| Clinical SAS Programmer - Remote but must be in EST or CST at Remote, Remote, USA |
| Email: [email protected] |
| From: Aman Chauhan, Source Infotech Inc. [email protected] Reply to: [email protected] Hi, Please find the details of Requirement. 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 Thanks, Aman Chauhan Team Lead (IT Recruitment) Source InfoTech Inc., Email: [email protected] Disclaimer: If you are not interested in receiving our e-mails then please reply with a "REMOVE" in the subject line at [email protected] for automatic removal. And mention all the e-mail addresses to be removed with any e-mail addresses, which might be diverting the e-mails to you. We are sorry for the inconvenience . Keywords: active directory rlang information technology Clinical SAS Programmer - Remote but must be in EST or CST [email protected] |
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| Fri Sep 20 19:57:00 UTC 2024 |