Overview Senior / Principal Statistical Programmer (Clinical SAS Programmer), South Africa. The role involves technical leadership in statistical programming for clinical trials, providing expert support and advising internal and external sponsors, and ensuring quality, timelines, and budgeting considerations are maintained. Responsibilities - Provide technical expertise for the conduct of...
A leading clinical research organization seeks a Senior Statistical Programmer to utilize advanced SAS skills and lead programming projects. The role requires a Master's degree in Statistics, at least 5 years of experience in Statistical Programming, and proficiency in E-Submission Standards. Candidates should exhibit good communication skills and a strong understanding of clinical trials. Join a...
A leading biostatistics organization in South Africa seeks a skilled SAS Programmer to provide technical leadership in analyzing clinical trial data. The ideal candidate will have a strong background in SAS programming, experience in the pharmaceutical industry, and excellent communication skills. This role involves ensuring compliance with regulations, performing quality control checks, and...
A clinical research organization in Bloemfontein seeks a Senior Statistical Programmer to program and validate statistical analysis of clinical studies with SAS. The role requires more than 3 years of experience in clinical programming and strong knowledge of CDISC SDTM and ADaM standards. A degree in relevant fields is necessary, as well as good communication skills in English. The company...
(Senior) Statistical Programmer (Bloemfontein, SA) Full-time Biometrie Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. As a growth-oriented medium-sized company with over 155 employees, we operate internationally. Our customers appreciate the...
A global healthcare intelligence firm is looking for a Senior Statistical Programmer II in Johannesburg, South Africa. You will be responsible for designing and developing SAS programs for clinical data analysis, ensuring accuracy and compliance with regulations. The ideal candidate should have a degree in Statistics or a related field and significant experience in the pharmaceutical industry....
An international research institute is seeking a Head of Policy Research for their SA-TIED programme in Pretoria, South Africa. The successful candidate will manage the programme, oversee local partnerships, and guide research initiatives and capacity development. A Master's degree in a relevant field is required, along with at least 5 years of relevant experience. The role offers an attractive...
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development...
A data-focused clinical research organization is seeking a Senior Statistical Programmer. This role requires mastery in SAS programming and a Master's degree. The ideal candidate will have over 5 years of experience in statistical programming and should have hands-on clinical trial experience. Responsibilities include generating data reports and leading programming projects. Join a supportive...
Statistical Programmer II (Clinical SAS Programmer), South Africa The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part...
A clinical research company in Bloemfontein is looking for a (Senior) Statistical Programmer to program and validate statistical analysis for clinical studies. Candidates should have over 3 years of experience in SAS programming, knowledge of CDISC standards, and strong communication skills in English. The company offers attractive remuneration, remote working options, and a supportive work...
(Senior) Statistical Programmer (Bloemfontein, South Africa) Your responsibilities - You program and validate statistical analysis of clinical studies with SAS. - You define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS. - You are responsible for the quality control of evaluations of clinical studies. - You conduct all other programming activities needed during a...
Overview Parexel is hiring for Statistical Programmer II and Senior Statistical Programmer roles as part of our growing Functional Service Provider (FSP) team. Responsibilities - Develop and validate SAS programs for datasets, tables, listings, and figures - Collaborate with global teams to support clinical trial analysis - Ensure compliance with CDISC standards and regulatory requirements -...
When our values align, there's no limit to what we can achieve. Overview The Senior / Principal Statistical Programmer overall duties include; Responsibilities - provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing...
A global clinical research organization is seeking a Senior / Principal Statistical Programmer to provide technical expertise for clinical trials in Pretoria, South Africa. This role includes responsibilities like leading programming activities and acting as a subject matter expert. Candidates must possess strong SAS programming skills with at least 3.5 years of experience and advanced project...
A leading life sciences consulting firm is seeking to fill the role of Statistical Programmer II/Senior Statistical Programmer. This role involves developing and validating SAS programs, ensuring compliance with CDISC standards, and collaborating with global teams within a flexible, remote-friendly environment. Candidates should have a minimum of 3 years of experience in clinical/statistical...
When our values align, there's no limit to what we can achieve. The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part...
When our values align, there's no limit to what we can achieve. The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part...
When our values align, there's no limit to what we can achieve. Parexel is hiring for Statistical Programmer II and Senior Statistical Programmer roles as part of our growing Functional Service Provider (FSP) team. 💡 What you’ll do: Develop and validate SAS programs for datasets, tables, listings, and figuresCollaborate with global teams to support clinical trial analysisEnsure compliance with...
When our values align, there's no limit to what we can achieve. Parexel is hiring for Statistical Programmer II and Senior Statistical Programmer roles as part of our growing Functional Service Provider (FSP) team. 💡 What you’ll do: Develop and validate SAS programs for datasets, tables, listings, and figuresCollaborate with global teams to support clinical trial analysisEnsure compliance with...