Hello,
Hope you are doing well,
Please go through the following requirement and let me know on Dhruv@riderconsultinginc.com if you have any available
Role SAS Programmers (Clinical)
Location MA or NC
Duration One Year
Job Description:
- Candidates will be expected to do both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software.
- Must be able to work with minimal supervision under the direction of a lead programmer.
- Must be able to effectively and timely communicate issues to lead programmer or manager.
- Must meet timelines or communicate proactively and effectively if timelines are at risk so that mitigating plans can be adjusted and/or executed.
- Will be expected to contribute to departmental process improvement initiatives.
- Contingent upon on experience work level, may lead a study.
Qualifications:
- Must be highly knowledgeable in the field of statistical programming.
- Must be able to handle a moderate to large volume of complex tasks with minimal supervision.
- Must have the ability to handle ad-hoc requests with minimal guidance.
- Must be able to recognize when negotiating skills are needed and seek assistance when necessary.
- Excellent organizational, interpersonal, and communication skills are a must; essential function of the role.
- 5 + years SAS programming including SAS STAT, GRAPH and MACRO
- 5 + years relevant industry experience
- Extensive knowledge of drug development process and clinical trials
- Extensive knowledge of drug submission requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards
- Educational Background requirements/expectations:
- Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.
Thanks,
Dhruv Soni
Phone : 218-656-0396
Email : Dhruv@riderconsultinginc.com
Gtalk : rider.dhruv1
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