Katalyst CRO
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Clinical SAS Programmer
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Katalyst CRO 1 week ago Be among the first 25 applicants Join to apply for the
Clinical SAS Programmer
role at
Katalyst CRO Providing statistical programming support to generate tables, listings, and figures for assigned projects. Demonstrating proficiency in CDISC, SDTM, and Adam to support various submission activities, including IA, CSR, DSUR, and publications. Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs. Creating detailed specifications for individual studies and comprehensive summaries. Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and Adam datasets. Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts. Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback. Validating datasets and tables through double programming. Having a good understanding of oncology-specific domains is an advantage.
Responsibilities
Providing statistical programming support to generate tables, listings, and figures for assigned projects. Demonstrating proficiency in CDISC, SDTM, and Adam to support various submission activities, including IA, CSR, DSUR, and publications. Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs. Creating detailed specifications for individual studies and comprehensive summaries. Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and Adam datasets. Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts. Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback. Validating datasets and tables through double programming. Having a good understanding of oncology-specific domains is an advantage.
Requirements:
A master's or bachelor's degree (or equivalent qualification) in a relevant field. At least 5 years of solid experience in statistical programming with clinical trial data, particularly using SAS software. A strong team player who is open to learning and adopting new methods and technologies, contributing positively to team dynamics. A quick learner with a proven history of effective collaboration and teamwork. Exceptional communication skills, both written and verbal. Demonstrated ability to multitask, prioritize, anticipate potential challenges, and achieve goals within a multidisciplinary team environment. Prior experience in oncology and vendor management is highly preferred. Seniority level
Seniority level Associate 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
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Clinical SAS Programmer
role at
Katalyst CRO 1 week ago Be among the first 25 applicants Join to apply for the
Clinical SAS Programmer
role at
Katalyst CRO Providing statistical programming support to generate tables, listings, and figures for assigned projects. Demonstrating proficiency in CDISC, SDTM, and Adam to support various submission activities, including IA, CSR, DSUR, and publications. Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs. Creating detailed specifications for individual studies and comprehensive summaries. Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and Adam datasets. Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts. Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback. Validating datasets and tables through double programming. Having a good understanding of oncology-specific domains is an advantage.
Responsibilities
Providing statistical programming support to generate tables, listings, and figures for assigned projects. Demonstrating proficiency in CDISC, SDTM, and Adam to support various submission activities, including IA, CSR, DSUR, and publications. Overseeing all aspects of statistical programming, working closely with statisticians to ensure timely and accurate delivery of statistical outputs. Creating detailed specifications for individual studies and comprehensive summaries. Directing and supervising CRO activities related to statistical programming, including the creation and validation of SDTM and Adam datasets. Producing safety tables, efficacy tables, and lab shift tables in accordance with the SAP and mock layouts. Reviewing statistical analysis plans, annotated CRFs, and integrated summaries, providing thoughtful feedback. Validating datasets and tables through double programming. Having a good understanding of oncology-specific domains is an advantage.
Requirements:
A master's or bachelor's degree (or equivalent qualification) in a relevant field. At least 5 years of solid experience in statistical programming with clinical trial data, particularly using SAS software. A strong team player who is open to learning and adopting new methods and technologies, contributing positively to team dynamics. A quick learner with a proven history of effective collaboration and teamwork. Exceptional communication skills, both written and verbal. Demonstrated ability to multitask, prioritize, anticipate potential challenges, and achieve goals within a multidisciplinary team environment. Prior experience in oncology and vendor management is highly preferred. Seniority level
Seniority level Associate 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
Dallas, TX . Virtual Data Analyst Full Time ( 100% Remote)
Dallas-Fort Worth Metroplex $20.00-$22.00 1 day ago Dallas, TX $60,000.00-$80,000.00 3 hours ago Virtual Data Analyst (Entry Level) (Remote)
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Dallas, TX $75,000.00-$85,000.00 4 days ago Dallas, TX $80,000.00-$90,000.00 16 hours ago Dallas, TX $100,000.00-$120,000.00 3 weeks ago Entry Level Data Analyst, application via RippleMatch
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr