Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support ...
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Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support ...
Quick apply
Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support ...
Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support ...
Quick apply
Senior SAS Programmer Senior Statistical Programmer * -Perform SAS data manipulation and analysis programming -May work with medical writing, clinical operations, and other clinical staff to support ...
Background in statistics and statistical analysis is desirable * 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming * Strong competence in SAS ...
Background in statistics and statistical analysis is desirable * 10 plus years Pharmaceutical or CRO industry experience in clinical reporting and statistical programming * Strong competence in SAS ...
Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.Phase 3 and regulatory submission experience preferred.Strong SAS ...
Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.Phase 3 and regulatory submission experience preferred.Strong SAS ...
Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.Phase 3 and regulatory submission experience preferred.Strong SAS ...
Minimum of 10 years of relevant statistical programming experience within the pharmaceutical, biotechnology, or CRO industry.Phase 3 and regulatory submission experience preferred.Strong SAS ...
Great Lakes, IL · On-site
Job Title The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians ...
Great Lakes, IL · On-site
Job Title The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. The successful candidate will work closely with the Biostatisticians ...
... Statistical Programming. The Sr. Associate, Biometrics Quality role will be responsible for ... IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I ...
... Statistical Programming. The Sr. Associate, Biometrics Quality role will be responsible for ... IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I ...
Great Lakes, IL · On-site
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
Great Lakes, IL · On-site
The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data. * The successful candidate will work closely with the Biostatisticians, Data ...
Irvine, CA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
Irvine, CA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
... SAS programming and statistical analyses using large medical claims data, electronic medical ... CRO health-related consulting company 2. At least 2 years of experience in large medical claims ...
... SAS programming and statistical analyses using large medical claims data, electronic medical ... CRO health-related consulting company 2. At least 2 years of experience in large medical claims ...
Irvine, CA · On-site
Minimum 6+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
Irvine, CA · On-site
Minimum 6+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
Irvine, CA · On-site
Minimum 6+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Experience in ...
Irvine, CA · On-site
Minimum 6+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. Experience in ...
Addison, TX · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
Addison, TX · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
Irvine, CA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
Irvine, CA · On-site
Minimum 7+ years' experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. * Experience using SAS-Base, MACRO, STAT, GRAPH, ACCESS, MS Office. * Experience in ...
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... statistical analysis, SAS programming, data management, medical writing, medical monitoring ...
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R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... statistical analysis, SAS programming, data management, medical writing, medical monitoring ...
San Diego, CA · On-site
$154.16K - $195K/yr
Minimum of BS required in Statistics, Computer Science, Life Sciences or other related fields. * BS with 7+ years or MS with 5+ years of SAS programming experience in drug development in CRO or ...
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San Diego, CA · On-site
$154.16K - $195K/yr
Minimum of BS required in Statistics, Computer Science, Life Sciences or other related fields. * BS with 7+ years or MS with 5+ years of SAS programming experience in drug development in CRO or ...
Somerset, NJ · On-site
$72K/yr
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... statistical analysis, SAS programming, data management, medical writing, medical monitoring ...
Quick apply
Somerset, NJ · On-site
$72K/yr
R&G US Inc. is a leading Contract Research Organization (CRO) providing full services for clinical ... statistical analysis, SAS programming, data management, medical writing, medical monitoring ...
Santa Monica, CA · On-site
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
Santa Monica, CA · On-site
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
$107.19K - $138.71K/yr
Demonstrates SAS programming proficiency. * Generates the production of statistical analysis ... Degree in Biostatistics/Computer Science or equivalent. * 5+ years of pharmaceutical/CRO experience.
$84.5K - $99.5K
3% of jobs
$99.5K - $114.4K
10% of jobs
$124.5K is the 25th percentile. Wages below this are outliers.
$114.4K - $129.4K
18% of jobs
The median wage is $144.3K / yr.
$129.4K - $144.3K
19% of jobs
$157.3K is the 75th percentile. Wages above this are outliers.
$144.3K - $159.3K
29% of jobs
$159.3K - $174.2K
10% of jobs
$174.2K - $189.2K
12% of jobs
$189.2K - $204.1K
0% of jobs
$204.1K - $219.1K
0% of jobs
$219.1K - $234K
0% of jobs
$234K - $249K
0% of jobs
$84.5K
$147.3K
$249K
Job Description
Company Descriptions:
Wizsolution is located in Princeton NJ, which is a leader in pharmaceutical recruitment and staffing. Our goal is to provide effective solutions for fulfilling your career potential. The mission of our company is to connect high talent and motivated candidates to technical positions from our partner companies.
Job descriptions:
Senior SAS Programmer
Senior Statistical Programmer
*
-Perform SAS data manipulation and analysis programming
-May work with medical writing, clinical operations, and other clinical staff to support deliverables.
-Must work well both independently and with team members.
-Needs to be able to be on-time with deliverables, and for those deliverables to be of quality.
-Works with Statistician and Statistical programmer to assure results are consistent with expectations, and Quality control procedures are followed.
-Plans and carefully documents differences between programming results between program developer and Statistical QC programmer.
-Confirms that tracking sheets are current for projects, and may also confirm that results are consistent with earlier generated results.
· MS with 3-5 +years of pharmaceutical industry experience.
· Strong collaboration abilities and ability to work as part of a highly skilled team.
· Experience in CDISC (SDTM, ADaM data sets)
· Skilled in analysis of safety, efficacy & biomarker data, with an understanding of multiplicity issues; immunology/CV background a plus.
· Experienced with standard and advanced statistical methods.
· Expertise in SAS required, S-Plus or R preferred, including advanced statistical analysis, data integration, graphing & simulation.
· Strong programming skills.
· Good understanding of regulatory requirements & clinical trial design.
· Knowledge of and ability to learn relevant clinical background and biomarker biology and incorporate these into statistical design, analysis & interpretation.
Preferred Qualifications:
Must have 3-5+ years SAS Programmer experience
SAS systems experience may include Base SAS, SAS/FSP,SAS SCL, Macro Facility, SAS/Graph, SAS / ODS, and SAS / Stat within a Windows operating system.
Job Type: Full-time
Sourced by ZipRecruiter
51 - 200 Employees
Princeton, NJ, US
2011