Hope you are doing great!!
I have an urgent requirement with our client. Please let me know your interest.
SAS Data Programmer / Analyst with Life Science Experience
Location – New jersey (remote until covid lift)
Client needs candidates worked on Clinical data / studies in Pharma setting
Job description:
- This position provides statistical input and project management for statistical activities in relation to clinical trials.
- Authoring statistical sections of reports, and contributing to concept protocols, case report forms and integrated clinical/statistical reports
- Primary authorship and responsibility for analysis plans and statistical reports
- Ability to coordinate and delegate the production of data displays in an efficient manner for inclusion in integrated clinical/statistical reports and other similar reports.
- Ensuring statistical and integrated clinical/statistical reports meet regulatory and company standards.
- Perform QA procedures on work performed by others such as Third-Party Providers
- Performs, presents and interprets data manipulations/processing and statistical analyses.
- Derives statistical conclusions and makes recommendations based on experimental results. •
- Liaise with customers to understand and help define requirements.
- Experienced and skilled in the statistical methods related to analyzing and reporting clinical trials
- Proficient in SAS programming related to dataset manipulation and statistical techniques
- Knowledge of Industry standards such as ICH and country specific regulatory requirements.
Qualification- PhD (Statistics, Biostatistics, or related field) – 3-5 years; or • Msc (Statistician, Biostatics, or related field) – 7+ years in pharmaceutical research and development, or equivalent.
Thanks & Regards
| Dev Chauhan Account Manager Tanisha Systems Inc Direct: 646-867-8810, Desk no. 212-729-6543 Ext 335 (EST) Email: devendra@tanishasystems.com Address:99 Wood Ave South Suite # 308,Iselin, NJ 08830 |
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