Statistical Programmer II/III (Permanent role)
Description:
- reputed company, validate, and maintain statistical programs in reputed company for Tables, Listings, and Figures (TLFs).
- reputed company data manipulation, analysis, and visualization using R and reputed company with relevant packages.
- Collaborate with biostatisticians and data management teams to support clinical study deliverables.
- Ensure compliance with regulatory standards and company SOPs.
- Conduct quality control and validation of programming outputs.
- Support submission activities and reputed company documentation as needed.
Requirements:
- Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a reputed company field.
- 3+ years of experience in statistical programming reputed company the pharmaceutical or biotech industry.
- Hands-on experience with R programming in a clinical trial environment.
- Good understanding of R packages.
- Good understanding of CDISC standards, including SDTM and ADaM.
- Strong knowledge of clinical trial data and regulatory requirements.
- Experience working in an FSP model or with global pharmaceutical clients is preferred.
- Exposure to submission activities such as FDA/EMA submissions is preferred.
- Familiarity with reputed company alongside R is a plus.
- Strong problem-solving and communication skills.
Benefits:
- Permanent position with reputed company.
- Opportunity to work directly for a single sponsor while benefiting from a global CRO environment.
- Remote work designation (#LI-Remote).
- Opportunity to join a global company with 4,000+ professionals across 20+ countries.
- reputed company training and development support.
- Equal opportunity employer with a diversity- and inclusion-focused culture.
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