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Principal Statistical Programmer, SAS/Cdisc, New Jersey
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Design, Support
Projektbeschreibung
Principal Statistical Programmer, SAS/CDISC, New Jersey
SAS, SAS Programming, Statistics, Biostatistics, Principal Level, CDISC, SDTM, ADAM, New Jersey
Global, growing company in the pharmaceutical industry located in New Jersey is looking for someone like you to be a new Principal Statistical Programmer!
You will immediately jump into a technical role, working on multiple projects in numerous therapeutic areas.
Opportunities provided with this role include, but are not limited to:
* Provide leadership for creating programs to analyze and report clinical trial data
* Design and implement programs used in Clinical Research and Development studies.
* Analyze Clinical Study design requirements to support the implementation of electronic systems.
* Validate systems and programs internally externally according to current regulatory requirements.
All applicants must meet the following requirements to be considered:
*Masters Degree in Computer Science or related field
*At least 4 years of relevant pharmaceutical developmental experience
*Minimum 1 year of Lead Programmer experience
*Excellent knowledge of clinical trial methodologies
*Outstanding verbal, written and interpersonal communication skills
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, Statistics, Biostatistics, Principal Level, CDISC, SDTM, ADAM, New Jersey
Global, growing company in the pharmaceutical industry located in New Jersey is looking for someone like you to be a new Principal Statistical Programmer!
You will immediately jump into a technical role, working on multiple projects in numerous therapeutic areas.
Opportunities provided with this role include, but are not limited to:
* Provide leadership for creating programs to analyze and report clinical trial data
* Design and implement programs used in Clinical Research and Development studies.
* Analyze Clinical Study design requirements to support the implementation of electronic systems.
* Validate systems and programs internally externally according to current regulatory requirements.
All applicants must meet the following requirements to be considered:
*Masters Degree in Computer Science or related field
*At least 4 years of relevant pharmaceutical developmental experience
*Minimum 1 year of Lead Programmer experience
*Excellent knowledge of clinical trial methodologies
*Outstanding verbal, written and interpersonal communication skills
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
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Kategorie:
Medien/Design, Sonstiges