... SAS programming activities. Develop standard / ad-hoc JReview /SAS programs to provide complex listings/reports to support Data Management and clinical functions to clean and review data for Oncology ...
... SAS programming activities. Develop standard / ad-hoc JReview /SAS programs to provide complex listings/reports to support Data Management and clinical functions to clean and review data for Oncology ...
Familiarity with clinical data management systems ... SAS programming experience a plus * Analytical and Communication skills * Planning and Co ...
Familiarity with clinical data management systems ... SAS programming experience a plus * Analytical and Communication skills * Planning and Co ...
SAS Programmer - Entry Level
Cincinnati, OH · On-site +1
SAS Programming experience required * Minimum 3.4 GPA Medpace Overview Medpace is a full-service ... lV clinical development services to the biotechnology, pharmaceutical, and medical device ...
SAS Programmer - Entry Level
Cincinnati, OH · On-site +1
SAS Programming experience required * Minimum 3.4 GPA Medpace Overview Medpace is a full-service ... lV clinical development services to the biotechnology, pharmaceutical, and medical device ...
SAS Analyst
Orlando, FL · On-site
This position will report directly to the Data and Analytics Manager and will provide analytical ... Background in SAS programming is paramount to success in this role, as well as a complete ...
SAS Analyst
Orlando, FL · On-site
This position will report directly to the Data and Analytics Manager and will provide analytical ... Background in SAS programming is paramount to success in this role, as well as a complete ...
SAS Programmer
Chicago, IL · On-site
REQUIRED Skills: 1. SAS Data Management Advanced suite, specifically Data Integration Studio 2. SAS Programming 3. ETL Required Experience Bachelor's degree or higher in Computer Science, Statistics ...
SAS Programmer
Chicago, IL · On-site
REQUIRED Skills: 1. SAS Data Management Advanced suite, specifically Data Integration Studio 2. SAS Programming 3. ETL Required Experience Bachelor's degree or higher in Computer Science, Statistics ...
SAS Programming experience required * Minimum 3.4 GPA Medpace Overview Medpace is a full-service ... lV clinical development services to the biotechnology, pharmaceutical, and medical device ...
SAS Programming experience required * Minimum 3.4 GPA Medpace Overview Medpace is a full-service ... lV clinical development services to the biotechnology, pharmaceutical, and medical device ...
SAS Analyst
Orlando, FL · On-site
This position will report directly to the Data and Analytics Manager and will provide analytical ... Background in SAS programming is paramount to success in this role, as well as a complete ...
SAS Analyst
Orlando, FL · On-site
This position will report directly to the Data and Analytics Manager and will provide analytical ... Background in SAS programming is paramount to success in this role, as well as a complete ...
Senior SAS Programmer
Okemos, MI · On-site
... management practices and conforms to departmental application development standards and systems ... programming standards, procedures and guidelines. · Perform other related assigned duties as ...
Quick apply
Senior SAS Programmer
Okemos, MI · On-site
... management practices and conforms to departmental application development standards and systems ... programming standards, procedures and guidelines. · Perform other related assigned duties as ...
Associate Director, Clinical and Statistical Programming
Seattle, WA · On-site
$185K - $228K/yr
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
Associate Director, Clinical and Statistical Programming
Seattle, WA · On-site
$185K - $228K/yr
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
He/she will provide critical input on the design and analysis of our clinical trial data so that ... Provide statistical support to other statisticians through the management of tasks at the trial ...
He/she will provide critical input on the design and analysis of our clinical trial data so that ... Provide statistical support to other statisticians through the management of tasks at the trial ...
Senior Programmer Analyst- Remote, US
$90K - $120K/yr
... management and database support or SAS Programming or Spotfire or Tableau development. * Good ... Basic knowledge of clinical trial process and data management, biometrics, and systems applications ...
Senior Programmer Analyst- Remote, US
$90K - $120K/yr
... management and database support or SAS Programming or Spotfire or Tableau development. * Good ... Basic knowledge of clinical trial process and data management, biometrics, and systems applications ...
Clinical Data Manager * Clinical Development Associates * SAS Programmer * and more!
Clinical Data Manager * Clinical Development Associates * SAS Programmer * and more!
... manage statistical programming activities that support drug development programs and regulatory ... Programming lead for clinical programs as needed. Hand-on programming work in SAS and other ...
... manage statistical programming activities that support drug development programs and regulatory ... Programming lead for clinical programs as needed. Hand-on programming work in SAS and other ...
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
... clinical SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment, with at least 7 years in a leadership or management role. Additional Skills/Experience: * The ideal ...
... clinical SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment, with at least 7 years in a leadership or management role. Additional Skills/Experience: * The ideal ...
... clinical SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment, with at least 7 years in a leadership or management role. Additional Skills/Experience: * The ideal ...
... clinical SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment, with at least 7 years in a leadership or management role. Additional Skills/Experience: * The ideal ...
... programming languages and tools, distributed database management systems, state-of-the-art ... Requirement: 1. Apply and demonstrate expertise with efficient DATA step, SQL programming and SAS ...
... programming languages and tools, distributed database management systems, state-of-the-art ... Requirement: 1. Apply and demonstrate expertise with efficient DATA step, SQL programming and SAS ...
Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...
Minimum 6 Years SAS Programming Experience supporting Phase 1-3 clinical trials in CRO or pharmaceutical industry. * Solid understanding of SDTM and ADaM implementation guidance, minimum 4 years of ...
... clinical data management staff and biostatisticians to address issues in Pinnacle 21 reports ... Experience: • Typically requires at least seven years' experience in statistical programming with ...
... clinical data management staff and biostatisticians to address issues in Pinnacle 21 reports ... Experience: • Typically requires at least seven years' experience in statistical programming with ...
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
Quick apply
Review data management plans, data transfer plans, and test EDC deployment to ensure readiness for ... Provide hands-on SAS programming support for key safety and efficacy analyses of clinical trials ...
Manager Clinical Sas Programming information
See salary details
$19.23 - $24.78
4% of jobs
$24.78 - $30.33
9% of jobs
$30.33 - $35.88
4% of jobs
$35.88 - $41.43
7% of jobs
$41.78 is the 25th percentile. Wages below this are outliers.
$41.43 - $46.98
9% of jobs
The median wage is $52.53 / hr.
$46.98 - $52.53
17% of jobs
$52.53 - $58.09
7% of jobs
$58.09 - $63.64
14% of jobs
$65.40 is the 75th percentile. Wages above this are outliers.
$63.64 - $69.19
12% of jobs
$69.19 - $74.74
10% of jobs
$74.74 - $80.29
7% of jobs
$19
$54
$80
How much do manager clinical sas programming jobs pay per hour?
What are popular job titles related to Manager Clinical Sas Programming jobs?
For Manager Clinical Sas Programming jobs, the most frequently searched job titles are:

Senior Clinical Systems Programmer (JReview), Data Operations
Woodcliff Lake, NJ • On-site
Full-time
Re-posted 4 days ago
Job description
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Accountable for setting up studies & developing standard programs to create reports, listings, graphs, metrics for clinical data management and other areas of clinical for data review and data cleaning to conduct clinical trials in Oncology area within JReview environment. Develop standard programs for patient profiles, standard and ad-hoc reports for data review using JReview & SAS to support the clinical teams. Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
Develop standard / ad-hoc JReview /SAS programs to provide complex listings/reports to support Data Management and clinical functions to clean and review data for Oncology trials.
Set up studies in JReview, develop & maintain programs, support users, and provide training for JReview.
Develop programs to provide metrics, graphs, patient profiles and ad-hoc reports for data review to support the clinical teams.
Design and develop macros, applications, and other utilities to expedite programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.
Develop and maintain the programs with proper documentation and testing using departmental standards.
Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming practice.
Strong SAS programming skills in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL;
Strong JReview skills in terms of program development, administration, maintenance, and user support;
Extensive experience of handling external data, e.g., laboratory data, PK, ECG,Tumor, etc.;
Knowledge of developing reporting or other applications using SAS;
Knowledge of data management process; Good understanding of data cleaning process;
Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG;
Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus;
Strong problem-solving skills;
Able to work independently and a team player; Good organizational and time management skills ;
Capable of communicating technical concepts
Good understanding of system development life cycles, GCP, and related Regulatory guidelines.
Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus!! Thank you for your time and for consideration. I look forward to hearing from you.
Regards,
Jasmine Jogewar
Sr. Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
(Direct) 732-844-8720| (F) 732-549-5549
www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996