Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Senior SAS/Cdisc Programmer - New Jersey Pharmaceutical Company
Eingestellt von Real Staffing Group aus Frankfurt am Main
Projektbeschreibung
Senior SAS/CDISC Programmer - New Jersey Pharmaceutical Company
SAS, SAS Programming, Senior, CDISC, SDTM, ADAM, Statistics, Biostatistics, New Jersey
Market leading pharmaceutical company is looking for an outstanding statistical programmer like you with strong hands-on CDISC/SDTM technical ability!
You will immediately get to provide lead Phase II-IV clincal trials in numerous therapeutic areas, while given the chance to report to the Director, Statistical Programming.
You will have the opportunity to:
Lead (hands-on) 5-6 projects in numerous therapeutic areas
Report to Director, Statistical Programming
Phase II-IV trials (upon time of start date)
Other opportunities you will be exposed to include, but are not limited to:
* Perform role of primary and validation statistical programmer on all assigned studies
* Create derived data set specifications for all assigned studies and integrated summaries.
* Function in a project leader role
* Oversee timelines, training, work assignments, and check quality of work performed
* Provide training, technical assistance, and mentoring to new statistical programmers
All requirements must be met below:
5 years SAS programming experience at a strong pharmaceutical company
Hands-on CDISC/SDTM/adAm modeling
Lead at least 3 studies in the past
M.S Computer Science or Statistics related discipline (B.S will be considered)
If you are interested in this exciting opportunity, please submit your resume directly to Shaun Abrams who can be reached at 212-707-8499. Applicants must have a very good technical background for this new opportunity with a growing company.
To find out more about Real Staffing please visit www.realstaffing.com
SAS, SAS Programming, Senior, CDISC, SDTM, ADAM, Statistics, Biostatistics, New Jersey
Market leading pharmaceutical company is looking for an outstanding statistical programmer like you with strong hands-on CDISC/SDTM technical ability!
You will immediately get to provide lead Phase II-IV clincal trials in numerous therapeutic areas, while given the chance to report to the Director, Statistical Programming.
You will have the opportunity to:
Lead (hands-on) 5-6 projects in numerous therapeutic areas
Report to Director, Statistical Programming
Phase II-IV trials (upon time of start date)
Other opportunities you will be exposed to include, but are not limited to:
* Perform role of primary and validation statistical programmer on all assigned studies
* Create derived data set specifications for all assigned studies and integrated summaries.
* Function in a project leader role
* Oversee timelines, training, work assignments, and check quality of work performed
* Provide training, technical assistance, and mentoring to new statistical programmers
All requirements must be met below:
5 years SAS programming experience at a strong pharmaceutical company
Hands-on CDISC/SDTM/adAm modeling
Lead at least 3 studies in the past
M.S Computer Science or Statistics related discipline (B.S will be considered)
If you are interested in this exciting opportunity, please submit your resume directly to Shaun Abrams who can be reached at 212-707-8499. Applicants must have a very good technical background for this new opportunity with a growing company.
To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges