$80,000–$100,000 Per Year
Statistical Analysis System (SAS), Data Analysis, Statistical Programming Languages, Statistics Software, Statistics, Biology, Biostatistics, Biotech and Pharmaceutical, Clinical Data, Clinical Data Management, Clinical Research, Clinical Trial, Clinical Trial Management, Data Science, Detail Oriented, Mentoring, Onboarding, Public Health,
- Education: Master’s degree or PhD in Biostatistics, Public Health (MPH), Epidemiology, Statistics, Bioinformatics, Biology, Pharmaceutical Sciences, or a highly quantitative field.
- Technical Proficiency: Foundational knowledge of SAS software (DATA steps, basic PROCs like PROC SQL, SORT, FREQ) OR a strong background in R/Python programming with a demonstrated capability to rapidly adapt to SAS.
- Analytical Skills: Solid understanding of linear regression, survival analysis, and basic statistical methodologies commonly used in clinical studies.
- Attention to Detail: Proven ability to manage complex data structures with high precision and an analytical mindset.
- Work Authorization: Open to CPT/OPT/STEM OPT extension candidates. The candidate must be based in the United States.
- SAS Programming: Assist in developing, testing, and executing SAS programs to import, clean, and transform clinical trial data from various electronic data capture (EDC) systems.
- Data Standards: Learn and implement CDISC standards, including standardizing raw data into SDTM and ADaM datasets under the guidance of senior programmers.
Outputs Generation: Participate in generating and quality-checking statistical outputs, including clinical summary tables, data listings, and figures (TLFs) for clinical study reports (CSR). - Data Validation: Perform double-programming and data validation to ensure consistency, accuracy, and compliance of clinical datasets with regulatory guidelines.
- Documentation: Document program specifications, metadata, and codebooks to maintain clear traceability for statistical analysis components.
- Collaboration: Partner with clinical data managers and senior biostatisticians to resolve data discrepancies and optimize database structures.
Performance Bonus, Paid Time-Off, Flexible Schedule, Work From Home
ClinPharma Clinical Research LLC is a growing clinical data solutions provider dedicated to supporting pharmaceutical pipelines and clinical trial data management. We are seeking a detail-oriented SAS Data Analyst to join our biostatistics and data programming team. This is a 100% fully remote position offering a competitive salary range of $80,000–$100,000 per year.
This role is ideal for highly motivated recent graduates or career changers from biostatistics, public health, or life science backgrounds who possess strong data logic and are eager to establish a long-term career in clinical data science. We provide a structured onboarding environment with professional mentorship to help you successfully transition and contribute to real-world clinical trial projects.
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ClinPharma Clinical Research LLC