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Lead Statistical Programmer - Full Time - Large CRO - New Jersey
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Consultant
Projektbeschreibung
Lead Statistical Programmer - Full Time -Large CRO - New Jersey
SAS, SAS Programming, Statistics, Biostatistics, Lead, CDISC, SDTM, ADAM, New Jersey, CRO, Pharmaceutical
Market leading, large CRO located in New Jersey with a robust drug pipeline is looking for YOU to be an outstanding lead statistical programmer!
You will immediately get to lead (hands-on) multiple projects in numerous therapeutic areas, while reporting to the Director of Statistical Programming.
Opportunities provided with this role include, but are not limited to:
- Providing technical leadership and project management for clinical trials
- Developing SAS programs for the management and reporting of clinical trial data
- Act as a Statistical Programming consultant to clients and internal customers
- Proactively participate in and/or lead process/quality improvement initiatives
All applicants must meet the following requirements to be considered:
- 5 years SAS programming experience at a strong company in the pharmaceutical industry
- Lead at least 3 studies in the past
- M.S Computer Science or Statistics related discipline
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, Lead, CDISC, SDTM, ADAM, New Jersey, CRO, Pharmaceutical
Market leading, large CRO located in New Jersey with a robust drug pipeline is looking for YOU to be an outstanding lead statistical programmer!
You will immediately get to lead (hands-on) multiple projects in numerous therapeutic areas, while reporting to the Director of Statistical Programming.
Opportunities provided with this role include, but are not limited to:
- Providing technical leadership and project management for clinical trials
- Developing SAS programs for the management and reporting of clinical trial data
- Act as a Statistical Programming consultant to clients and internal customers
- Proactively participate in and/or lead process/quality improvement initiatives
All applicants must meet the following requirements to be considered:
- 5 years SAS programming experience at a strong company in the pharmaceutical industry
- Lead at least 3 studies in the past
- M.S Computer Science or Statistics related discipline
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:
Organisation/Management