Hi,
We have potential openings for the following skills with one of our client. Please let us know your interest by sending a copy of your resume in MS
Word format.
Full Name:
Current Location:
Contact:
Email:
Legal Status:
Last 4 digit SSN:
Skype ID for webcam interview:
Availability to start:
Relocation:
Rate:
Couple of References:
Reference:1
Name :
Designation :
Email ID:
Contact :
Reference:2
Name :
Designation :
Email ID:
Contact :
SR Statistical Programmer
Location: Florham Park, NJ
Duration: 12+ Months
Responsibilities
· Writing SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create CDISC SDTM/ADaM datasets
· Generate Define tables and annotated CRFs as per the CDISC and FDA specifications and guidelines
· Program in SAS for study report tables/listings/figures, and submitting the results of clinical trials for investigational medications
· CDISC SDTM and AdaM models and transforming raw data into these standards
· Support data management by generating data listings
· Conduct QC/Validation of SAS code and output produced by other Statistical Programmer
· Work in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards
· Utilize SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
· Create all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/ISE
Qualifications
· 6+ years of industry experience in SAS programming
· Excellent programming skill using SAS/STAT, SAS Macro, SAS/SQL, SAS/GRAPH
· Good knowledge of 21CFR11 and GCP
--
Thanks and Regards,
BenLee
Sr. Recruiter
Vectorsoft
| Email: Ben@vectorsoft.com |
We have potential openings for the following skills with one of our client. Please let us know your interest by sending a copy of your resume in MS
Word format.
Full Name:
Current Location:
Contact:
Email:
Legal Status:
Last 4 digit SSN:
Skype ID for webcam interview:
Availability to start:
Relocation:
Rate:
Couple of References:
Reference:1
Name :
Designation :
Email ID:
Contact :
Reference:2
Name :
Designation :
Email ID:
Contact :
SR Statistical Programmer
Location: Florham Park, NJ
Duration: 12+ Months
Responsibilities
· Writing SAS programs from instructions provided by Biostatisticians and Statistical Programmers to create CDISC SDTM/ADaM datasets
· Generate Define tables and annotated CRFs as per the CDISC and FDA specifications and guidelines
· Program in SAS for study report tables/listings/figures, and submitting the results of clinical trials for investigational medications
· CDISC SDTM and AdaM models and transforming raw data into these standards
· Support data management by generating data listings
· Conduct QC/Validation of SAS code and output produced by other Statistical Programmer
· Work in a team environment providing technical leadership and solving clinical trial reporting problems of moderate to high complexity within budget and customary time line constraints while assuring high quality standards
· Utilize SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH
· Create all files, documents, and analyses necessary to support an electronic submissions in eCTD format, including ISS/ISE
Qualifications
· 6+ years of industry experience in SAS programming
· Excellent programming skill using SAS/STAT, SAS Macro, SAS/SQL, SAS/GRAPH
· Good knowledge of 21CFR11 and GCP
--
Thanks and Regards,
BenLee
Sr. Recruiter
Vectorsoft
| Email: Ben@vectorsoft.com |
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