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Clinical Sas Programmers - New Jersey
Eingestellt von Real Staffing Group aus Frankfurt am Main
Gesuchte Skills: Design, Sql
Projektbeschreibung
Description:
Design, develop, and validate SAS programs for the generation of data tables, listings, and figures for clinical study reports, and integrated analyses. Be able to communicate effectively within a multi-disciplinary project team, and to effectively organize and manage multiple assignments with tight timelines
Responsibilities:
*Experience of creating and validating large complex integrated clinical trial data in CDISC format (SDTM / ADaM) with knowledge of clinical trial data management
*Experience creating and validating tables, listings, graphs using SAS/BASE, SAS/STAT, SAS/Macro, SAS/SQL, and SAS/GRAPH; use of S-Plus for graphs is a plus
*Design, develop, and validate SAS programs for creation of standard datasets.
* Develop data transfer specifications for external data transfers.
*Interact, as needed, with external data vendors (e.g., eCRF, laboratory, PK).
*Evaluate data, results and/or document findings; interact with other programmers and departments to provide and recommend solutions on clinical programming and/or clinical data issues.
*Provide direction to other clinical programming employees. Receive no instruction on routine assignments and minimal instruction on new assignments.
*Comply with Company SOPs and departmental guidelines and procedures.
Requirements:
*6 years+ of Clinical Programming experience.
*Bachelors degree in mathematics, statistics, or similar combination of education and experience.
*Fundamental knowledge of clinical programming principles, including familiarity with SAS, is required.
*NDA submission experience.
Please send resumes to me directly at '' with subject line 'Clinical SAS Programmer -New Jersey'
REFERRALS WELCOME!!
Call or email me if you have any questions at all 212-707-8499
Thanks
Paul Dai
To find out more about Real Staffing please visit www.realstaffing.com
Design, develop, and validate SAS programs for the generation of data tables, listings, and figures for clinical study reports, and integrated analyses. Be able to communicate effectively within a multi-disciplinary project team, and to effectively organize and manage multiple assignments with tight timelines
Responsibilities:
*Experience of creating and validating large complex integrated clinical trial data in CDISC format (SDTM / ADaM) with knowledge of clinical trial data management
*Experience creating and validating tables, listings, graphs using SAS/BASE, SAS/STAT, SAS/Macro, SAS/SQL, and SAS/GRAPH; use of S-Plus for graphs is a plus
*Design, develop, and validate SAS programs for creation of standard datasets.
* Develop data transfer specifications for external data transfers.
*Interact, as needed, with external data vendors (e.g., eCRF, laboratory, PK).
*Evaluate data, results and/or document findings; interact with other programmers and departments to provide and recommend solutions on clinical programming and/or clinical data issues.
*Provide direction to other clinical programming employees. Receive no instruction on routine assignments and minimal instruction on new assignments.
*Comply with Company SOPs and departmental guidelines and procedures.
Requirements:
*6 years+ of Clinical Programming experience.
*Bachelors degree in mathematics, statistics, or similar combination of education and experience.
*Fundamental knowledge of clinical programming principles, including familiarity with SAS, is required.
*NDA submission experience.
Please send resumes to me directly at '' with subject line 'Clinical SAS Programmer -New Jersey'
REFERRALS WELCOME!!
Call or email me if you have any questions at all 212-707-8499
Thanks
Paul Dai
To find out more about Real Staffing please visit www.realstaffing.com
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Medien/Design