9 Sas Programming jobs in South Africa

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests.

In this role, you will develop and validate SAS programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative Oncology drugs. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country.

What else can you expect from us?

• Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
• Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
• A genuine work life balance
• Flexibility in working hours
• A thorough onboarding with support from your personal mentor
• A permanent employment contract with Fortrea
• Excellent training and career development opportunities, as well as support with advancing your individual education
• Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide

Your responsibilities:

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
• Respond to QA and client audits and support qualification audits
• Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
• Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)

Your profile:

• Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
• In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials
• Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company
• Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
• Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs
• Solid knowledge of CDISC standards
• Prior experience working on oncology data (safety and efficacy) and/or on vaccine trials
• Submission experience is ideal
• Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail
• Business fluency in English – both spoken and written – is a must

REMOTE

#LI-AA3

#J-18808-Ljbffr

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests. In this role, you will develop and validate SAS programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative Oncology drugs. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers! You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country. What else can you expect from us? Rewarding and meaningful work in an established, diverse, highly profitable and respected global company Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc. A genuine work life balance Flexibility in working hours A thorough onboarding with support from your personal mentor A permanent employment contract with Fortrea Excellent training and career development opportunities, as well as support with advancing your individual education Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide Your responsibilities: Review SAPs and TFL shells from a programming perspective Advise on the development of complex TFL shells from a programming perspective Develop and/or lead the development of complex specifications for SDTMs and ADa M datasets Develop and maintain SAS programs to create SDTM and ADa M datasets and TFLs, and perform quality control of SDTM, ADa Ms and TFLs Produce / define XML / PDFs, Analysis Results Metadata (ARM), a CRFs and Reviewers Guides to support SDTMs and ADa Ms Respond to QA and client audits and support qualification audits Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) Your profile: Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs Proven professional experience with SDTMs, ADa M datasets (safety and efficacy) and TFLs Solid knowledge of CDISC standards Prior experience working on oncology data (safety and efficacy) and/or on vaccine trials Submission experience is ideal Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail Business fluency in English – both spoken and written – is a must REMOTE #LI-AA3 #J-18808-Ljbffr

As a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and support submissions, regulatory questions, publications as well as ad hoc and post hoc requests. In this role, you will develop and validate SAS programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative Oncology drugs. Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers! You can be 100% home-based in EMEA or, if you prefer, you can work from our local office in your home country. What else can you expect from us? Rewarding and meaningful work in an established, diverse, highly profitable and respected global company Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc. A genuine work life balance Flexibility in working hours A thorough onboarding with support from your personal mentor A permanent employment contract with Fortrea Excellent training and career development opportunities, as well as support with advancing your individual education Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide Your responsibilities: Review SAPs and TFL shells from a programming perspective Advise on the development of complex TFL shells from a programming perspective Develop and/or lead the development of complex specifications for SDTMs and ADa M datasets Develop and maintain SAS programs to create SDTM and ADa M datasets and TFLs, and perform quality control of SDTM, ADa Ms and TFLs Produce / define XML / PDFs, Analysis Results Metadata (ARM), a CRFs and Reviewers Guides to support SDTMs and ADa Ms Respond to QA and client audits and support qualification audits Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) Your profile: Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs Proven professional experience with SDTMs, ADa M datasets (safety and efficacy) and TFLs Solid knowledge of CDISC standards Prior experience working on oncology data (safety and efficacy) and/or on vaccine trials Submission experience is ideal Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail Business fluency in English – both spoken and written – is a must REMOTE #LI-AA3 #J-18808-Ljbffr

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

As a Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies.

In this role, you will develop and validate SAS and R programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team.

This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases . Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers!

What else can you expect from us?

• Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
• Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
• A genuine work life balance
• Flexibility in working hours
• A thorough onboarding with support from your personal mentor
• A permanent employment contract with Fortrea
• Excellent training and career development opportunities, as well as support with advancing your individual education
• Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide

Your responsibilities:

• Review SAPs and TFL shells from a programming perspective
• Advise on the development of complex TFL shells from a programming perspective
• Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets
• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs
• Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs
• Respond to QA and client audits and support qualification audits
• Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business
• Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs)

Your profile:

• Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
• In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials
• Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company
• Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs
• Programming experience in R is required
• Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs
• Solid knowledge of CDISC standards
• Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail
• Business fluency in English – both spoken and written – is a must

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

#J-18808-Ljbffr

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. As a Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. In this role, you will develop and validate SAS and R programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases . Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers! What else can you expect from us? Rewarding and meaningful work in an established, diverse, highly profitable and respected global company Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc. A genuine work life balance Flexibility in working hours A thorough onboarding with support from your personal mentor A permanent employment contract with Fortrea Excellent training and career development opportunities, as well as support with advancing your individual education Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide Your responsibilities: Review SAPs and TFL shells from a programming perspective Advise on the development of complex TFL shells from a programming perspective Develop and/or lead the development of complex specifications for SDTMs and ADa M datasets Develop and maintain SAS programs to create SDTM and ADa M datasets and TFLs, and perform quality control of SDTM, ADa Ms and TFLs Produce / define XML / PDFs, Analysis Results Metadata (ARM), a CRFs and Reviewers Guides to support SDTMs and ADa Ms Respond to QA and client audits and support qualification audits Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) Your profile: Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs Programming experience in R is required Proven professional experience with SDTMs, ADa M datasets (safety and efficacy) and TFLs Solid knowledge of CDISC standards Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail Business fluency in English – both spoken and written – is a must Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. #J-18808-Ljbffr

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. As a Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. In this role, you will develop and validate SAS and R programs for data presentations and analyses, and provide programming support to your multidisciplinary global project team. This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas such as chronic and rare diseases . Your expertise and your work as a statistical programmer has a direct impact on improving the health and lives of thousands of patients around the globe every day. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers! What else can you expect from us? Rewarding and meaningful work in an established, diverse, highly profitable and respected global company Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc. A genuine work life balance Flexibility in working hours A thorough onboarding with support from your personal mentor A permanent employment contract with Fortrea Excellent training and career development opportunities, as well as support with advancing your individual education Strong support from your Line Manager and your team, as well as from more than 20,000 Fortrea colleagues worldwide Your responsibilities: Review SAPs and TFL shells from a programming perspective Advise on the development of complex TFL shells from a programming perspective Develop and/or lead the development of complex specifications for SDTMs and ADa M datasets Develop and maintain SAS programs to create SDTM and ADa M datasets and TFLs, and perform quality control of SDTM, ADa Ms and TFLs Produce / define XML / PDFs, Analysis Results Metadata (ARM), a CRFs and Reviewers Guides to support SDTMs and ADa Ms Respond to QA and client audits and support qualification audits Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business Maintain awareness of industry standards, global regulatory requirements, internal guidelines and Standard Operating Procedures (SOPs) Your profile: Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: an equivalent completed vocational training and / or equivalent professional experience in statistical programming for clinical trials Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs Programming experience in R is required Proven professional experience with SDTMs, ADa M datasets (safety and efficacy) and TFLs Solid knowledge of CDISC standards Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail Business fluency in English – both spoken and written – is a must Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. #J-18808-Ljbffr

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SUMMARY:

SAS Developer with a keen interest in data analytics. Tertiary qualification and SAS certification. 18 month contract. Sound understanding of SAS programming and ETL concepts.

Recruiter:

People Source

Job Ref:

AW

Date posted:

Thursday, June 26, 2025

Location:

Johannesburg, South Africa

Salary:

Negotiable on experience

SUMMARY:

SAS Developer with a keen interest in data analytics. Tertiary qualification and SAS certification. 18 month contract. Sound understanding of SAS programming and ETL concepts.

POSITION INFO:

At least 5 years experience as an Application Developer with a focus on SAS programming and data analytics. Banking industry experience an advantage. Develop, maintain and enhance the SAS environment, integrate SAS with other systems and drive the data-driven initiatives. Gauteng based.

Seniority level

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Employment type

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Join to apply for the SAS Developer - 18 month contract role at Executive Placements.com - The JOB Portal 3 days ago Be among the first 25 applicants Join to apply for the SAS Developer - 18 month contract role at Executive Placements.com - The JOB Portal Get AI-powered advice on this job and more exclusive features. SUMMARY:SAS Developer with a keen interest in data analytics. Tertiary qualification and SAS certification. 18 month contract. Sound understanding of SAS programming and ETL concepts. Recruiter:People SourceJob Ref:AWDate posted:Thursday, June 26, 2025Location:Johannesburg, South AfricaSalary:Negotiable on experienceSUMMARY:SAS Developer with a keen interest in data analytics. Tertiary qualification and SAS certification. 18 month contract. Sound understanding of SAS programming and ETL concepts.POSITION INFO:At least 5 years experience as an Application Developer with a focus on SAS programming and data analytics. Banking industry experience an advantage. Develop, maintain and enhance the SAS environment, integrate SAS with other systems and drive the data-driven initiatives. Gauteng based.Seniority level Seniority level Mid-Senior level Employment type Employment type Contract Job function Job function Information Technology Industries Advertising Services Referrals increase your chances of interviewing at Executive Placements.com - The JOB Portal by 2x Sign in to set job alerts for “SAS Developer” roles. Johannesburg, Gauteng, South Africa 1 week ago Bedfordview, Gauteng, South Africa 3 weeks ago Sandton, Gauteng, South Africa 3 days ago Sandton, Gauteng, South Africa 2 months ago Sandton, Gauteng, South Africa 1 month ago Johannesburg, Gauteng, South Africa 6 months ago Johannesburg Metropolitan Area 1 week ago City of Johannesburg, Gauteng, South Africa 2 weeks ago Junior / Intermediate Software Developer Johannesburg, Gauteng, South Africa 3 days ago Sandton, Gauteng, South Africa 3 days ago Johannesburg, Gauteng, South Africa 1 day ago Johannesburg, Gauteng, South Africa 3 days ago Midrand, Gauteng, South Africa 2 weeks ago Johannesburg, Gauteng, South Africa 1 week ago Johannesburg Metropolitan Area 1 month ago Sandton, Gauteng, South Africa 3 weeks ago Woodmead, Gauteng, South Africa 1 month ago Johannesburg, Gauteng, South Africa 2 days ago Johannesburg, Gauteng, South Africa 3 days ago Johannesburg, Gauteng, South Africa 3 days ago Johannesburg, Gauteng, South Africa 1 week ago Johannesburg, Gauteng, South Africa 1 week ago Johannesburg Metropolitan Area 2 days ago Johannesburg, Gauteng, South Africa 1 year ago Johannesburg, Gauteng, South Africa 9 months ago Ivory Park, Gauteng, South Africa 1 month ago City of Johannesburg, Gauteng, South Africa 1 day ago Johannesburg, Gauteng, South Africa 3 days ago 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