Friday, August 10, 2012

Sr. Stat Programmer job at Ockham in Lenexa

Ockham is at present looking to employ Sr. Stat Programmer on Fri, 10 Aug 2012 13:48:31 GMT. Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget. One of our clients in Lenexa, KS is looking for aSr. Stat Programmer. This is a contract position.Statistical Programmer with Nonmem experience required for a 6...

Sr. Stat Programmer

Location: Lenexa Kansas

Description: Ockham is at present looking to employ Sr. Stat Programmer right now, this job will be placed in Kansas. Further informations about this job opportunity kindly see the descriptions. Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget. One of our clients in Lenexa, KS is looking for aSr. Stat Programmer. This is a contract position.Statistical Programmer with Nonmem experience required for a 6 month contract.Develop TLF's for Phase I studies.Create CDISC compliant datasets.Develop submission ready documentation.Create polpulation PK Nonment datasets with supporting outputs. 5 years of Statistical Programming experience in the Pharmaceutical/CRO industryPK experienceNONMEM experienceKeywords: SAS, SAS Programmer, Statistics, Statistical Programmer, Statistical Analysis, ISS/ISE, Biostatistician, Biostatistical Programmer, Clinical Trials, Clinical Research, Clinical Studies, Pharmaceuticals, Drug Development, IND, NDA, Data Management, Data Manager, Clinical Data Manager, Clinical Data Coordinator, Drug Safety, Drug Safety Specialist, Drug Safety Associate, Pharmacovigilence, Drug Safety Nurse, Drug Safety Physician, Medical Writer, Medical Writing, Regulatory Affairs, Regulatory Submissions, Clinical Project Manager, Clinical Trials Specialist, Medical Services Specialist, BSN, RN, Clinical Research Associate, CRA, Clinical Study Manager, Clinical Study Monitor, Clinical Trials Monitoring, Regional CRA, Regional Clinical Research Associate, In-house CRA, In-house Clinical Research Associate, CDISC, SDTM, ADaM, Rave, Medidata, InForm, Home based, telecommuting, ASG, Ockham
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If you were eligible to this job, please email us your resume, with salary requirements and a resume to Ockham.

If you interested on this job just click on the Apply button, you will be redirected to the official website

This job starts available on: Fri, 10 Aug 2012 13:48:31 GMT



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