Senior Statistical Programmer

April 11

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ERGOMED

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ERGOMED is a global group providing specialized services to the biotechnology and pharmaceutical industries. It operates under different service lines, including Ergomed Clinical Research, PrimeVigilance, and ADAMAS Consulting, and is dedicated to providing full-service clinical research organization (CRO) capabilities. Focused on oncology, rare diseases, and complex trials, it also offers end-to-end pharmacovigilance and medical information services, as well as comprehensive GxP audits. Ergomed is committed to supporting drug development with a global presence in around 100 countries.

Oncology • Neurology • Respiratory diseases • Orphan drugs • Metabolic diseases

1001 - 5000 employees

Founded 1997

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• The Senior Statistical Programmer (SP) within the Ergomed Biostatistics (BS) department is responsible for the creation of SDTM/ADaM datasets and programming tables, listings and figures or other types of output. • The Senior Statistical Programmer is accountable for the first-time quality of the product, either dataset or output, via thorough QC steps. • Maintains responsibility for all assigned duties within a clinical study, this may include ensuring that work is performed on time. • Works with other biometrics’ team members to represent the needs and input of the programming components of the study. • Program SDTM and ADaM datasets Create SDTM and ADaM specifications Create CDISC submission packages. • Deliver training and mentorship to SP and other operational staff, as applicable. • Contribute to the development of the department in supporting adherence to good programming and best practices. • Act as a statistical programming expert and provide consultative support to internal programmers and biostatisticians • Assist their manager with programming work projections to aid departmental planning.

🎯 Requirements

• Bachelor's Degree, preferably in Computer Science, Mathematics/Statistics, or a quantitative natural science. • Extensive knowledge of SAS programming and statistical programming topics relevant to clinical trials • Advanced CDISC knowledge • Hands-on experience using P21E • 8 - 10 years’ of experience in developing derived datasets, TFL programming and submission packages in Clinical Research • Organization skills, including attention to detail and multitasking • Communication skills • Knowledge of the MS Office Suite • Proficiency in one or more statistical programming languages (includes SAS, R)

🏖️ Benefits

• Training and career development opportunities internally • Strong emphasis on personal and professional growth • Friendly, supportive working environment • Opportunity to work with colleagues based all over the world, with English as the company language