- Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets for accurate reporting and submission purposes.
- Develop, validate, and maintain high-quality Tables, Listings, and Figures (TLFs) for clinical study reports.
- Write efficient SAS programs for data cleaning, derivations, and reporting with strong attention to documentation practices.
- Familiarity with Python or R programming languages is an asset for automation tasks.
- A solid background in SAS programming language along with hands-on experience in CDISC standards (SDTM & ADaM).
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<b>Data Analytics Expert For Regulatory Compliance</b> - Pinhais, PR - beBeeClinicalDataAnalyst
Título do emprego: Clinical Statistical Programmer
Descrição
Clinical Data Analyst - CDISC Standards
We are seeking a detail-oriented Clinical Data Analyst to support clinical trial data standardization, analysis, and regulatory submissions.
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Estágio - Compliance
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Manager, Vendor Strategy and Operations
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Technical Product Manager (OTE 70,000/year USD), Finance
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Analista de Facilities e Segurança SR
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Product Manager: Payments Mandates
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Product Manager: Payments Mandates
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