Programmer and Statistican Opportunities - Pharmaceutical

From sasCommunity

Good morning!

How are you? I just had a position come across my desk that I thought you or someone you know may be interested in. I have listed the details below. I also have other positions available if these are not of interest.

I can also offer you a $1000 referral bonus for candidates that are placed on either of these orders. Please contact me for details.

Thank you and I look forward to hearing from you.

Company  : GlaxoSmithKline Job Title  : Statisticians and Statistical Programmers Location  : King of Prussia, PA & Durham, NC Length  : Long term contracts!!!! We have contractors that have been working with this group for 10 years!!!!!

Statisticians Authoring statistical sections of reports, and contributing to concept protocols, protocols, case report forms and integrated clinical/statistical reports. Primary authorship and responsibility for analysis plans and statistical analyses, tabulations, graphics and listings of clinical trial data. 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 quality assurance procedures on work performed by others. 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. Represent Biometrics at Investigator Meetings, internal teams, contract organizations and external regulatory agencies. Work independently; attention to detail; team player. MS degree in Biostatistics or related field. Minimum of 3 years related experience within the Contract Research Organization (CRO) or pharmaceutical/clinical trials environment.

Statistical Programmers Must have strong MACRO and efficacy experience. Provide statistical programming expertise (preferably in SAS) in the production of analyses, tabulations, graphics, and listings from clinical trial data. Key responsibilities and skills include, but are not limited to, the following: Contribute to the preparation of analysis plans. Prepare, document and test required programs and procedure data displays in an efficient manner for inclusion in integrated clinical statistical reports and other similar reports. Contribute to the integrated clinical/statistical report and other similar documents. Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming and reporting. Perform quality assurance procedures on work performed by others. Work independently; attention to detail; team player. MS degree in Biostatistics or related field. Minimum of 3 years related experience within the Contract Research Organization (CRO) or pharmaceutical/clinical trials environment.

Sincerely, Catherine Zeier (Capone) Team Leader ClinForce, LLC. czeier@clinforce.com (800) 964-2877 x33867 (toll-free) (919) 433-3867 (direct line) (407) 518-9294 (fax)