Katalyst CRO
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Sr. SAS Programmer
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Katalyst CRO 4 weeks ago Be among the first 25 applicants Join to apply for the
Sr. SAS Programmer
role at
Katalyst CRO To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g. Publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors to develop or monitor the content and structure of SAS data sets. Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Maintaining standards for programming activities. Working independently to accomplish tasks and goals defined by supervisor. Bringing in new ideas to improve the programming process.
Responsibilities
To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g. Publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors to develop or monitor the content and structure of SAS data sets. Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Maintaining standards for programming activities. Working independently to accomplish tasks and goals defined by supervisor. Bringing in new ideas to improve the programming process.
Requirements:
Minimum of bachelor's degree in related science discipline. 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 CDISC data standards, e.g. SDTM and ADaM. Proven experience with Unix and Windows operating systems. Understanding of the software development life cycle. Understanding of FDA guidelines. Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. Applies good judgment and demonstrates initiative to resolve issues. Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Contract Job function
Job function
Information Technology Industries
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Sr. SAS Programmer
role at
Katalyst CRO 4 weeks ago Be among the first 25 applicants Join to apply for the
Sr. SAS Programmer
role at
Katalyst CRO To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g. Publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors to develop or monitor the content and structure of SAS data sets. Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Maintaining standards for programming activities. Working independently to accomplish tasks and goals defined by supervisor. Bringing in new ideas to improve the programming process.
Responsibilities
To support the Biostatistics team by carrying out programming activities of statistical programmers and overseeing external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies and publications. Contributes to the overall efficiency and best practice of the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Providing statistical programming and validation support for clinical study reports, overseeing programming activities by external vendors (e.g., CROs) when necessary and coordinating programming activities among the study programmers to achieve timely progress in the following areas: SDTM datasets, ADaM datasets, statistical tables, figures, listings, and other internal and external requests (e.g. Publications). Accessing and converting data to SAS from Database management system and PC file formats (e.g., MS Excel, text files). Working with external vendors to develop or monitor the content and structure of SAS data sets. Working closely with clinicians, statistician, and publication managers to generate and QC outputs for publications; review publication (abstract/manuscripts) to ensure accuracy, quality and soundness of statistical methodologies; coordinate internal resource utilization for publication and generate activities metrics for management review. Providing input to the Database and CRF Development, creating edit check programs and providing feedback to the Data Management. Providing input in developing statistical analysis plans, specifications of analysis datasets, validation plans, and other related documents. Maintaining standards for programming activities. Working independently to accomplish tasks and goals defined by supervisor. Bringing in new ideas to improve the programming process.
Requirements:
Minimum of bachelor's degree in related science discipline. 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 CDISC data standards, e.g. SDTM and ADaM. Proven experience with Unix and Windows operating systems. Understanding of the software development life cycle. Understanding of FDA guidelines. Good organization, time management and attention to detail skills needed to work in a stressful environment under tight deadlines while maintaining focus on details and quality. Applies good judgment and demonstrates initiative to resolve issues. Strong verbal, written and interpersonal communication skills needed to work effectively in a team environment. Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Contract Job function
Job function
Information Technology Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Get notified about new SAS Developer jobs in
Irvine, CA . Irvine, CA $74,859.00-$100,227.00 2 weeks ago Irvine, CA $120,000.00-$135,000.00 13 hours ago Irvine, CA $70,694.00-$81,492.00 2 weeks ago Irvine, CA $82,382.00-$110,272.00 1 week ago Data Analyst I (North America Quality Center - NAQC)
Irvine, CA $70,000.00-$78,000.00 2 days ago Irvine, CA $75,000.00-$82,000.00 4 days ago Data Analyst (North America Quality Center - NAQC)
Irvine, CA $70,000.00-$93,000.00 2 days ago Irvine, CA $99,461.00-$128,329.00 1 week ago Data Analyst III - Transportation Management Systems
Irvine, CA $105,000.00-$136,000.00 1 week ago Associate Analyst, Data-Remote in California
Newport Beach, CA $70,000.00-$115,000.00 2 weeks ago Analyst - Excel Reports (Advanced level/Power user), Data
Irvine, CA $87,316.74-$117,873.05 3 weeks ago Aliso Viejo, CA $61,000.00-$86,000.00 1 month ago Santa Fe Springs, CA $100,000.00-$120,000.00 1 week ago Long Beach, CA $4,469.00-$6,922.00 1 week ago Data Analyst, Sr. (Finance - Encounter Data)
Orange, CA $84,092.00-$134,548.00 4 days ago Software Engineer II, Data Analysis Tools
Long Beach, CA $141,000.00-$180,000.00 1 week ago Clinical Operations Data Analyst - Enterprise Data and Analytics - FT - Day - Remote
Clinical Operations Data Analyst - Enterprise Data and Analytics - FT - Day - Remote
Irvine, CA $147,900.00-$184,900.00 5 days ago Long Beach, CA $90,000.00-$110,000.00 2 months ago Orange, CA $149,882.00-$224,823.00 2 weeks ago Data Analyst - Managed Care Operations - Remote CA
Long Beach, CA $68,640.00-$111,967.00 1 month ago Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr