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- Employment type
- Full-time
- Experience level
- Senior · 5+ years
- Minimum education
- Bachelor’s degree
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Mid-Senior level
- Application method
- Apply on LinkedIn (LinkedIn sign-in required)
Job summary
The Senior Statistical Analyst I will develop and validate complex analysis datasets and TFLs using SAS, while also serving as a project lead programmer. Responsibilities include writing programming specifications, mentoring team members, and ensuring compliance with regulatory standards.
Job details
Key Responsibilities Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. Write and review programming specifications and supporting documentation. Create standard macros and tools to improve efficiency. Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members. Communicate with clients as the key programming contact, including delivering outputs and managing feedback. Conduct SAS code review, track issues, and ensure quality standards are met. Archive all programming deliverables and documentation per SOPs. Mentor team members and support their technical and professional development. Ensure compliance with ICH-GCP, CDISC standards, and company SOPs. Requirements Bachelor’s degree or above in Statistics, Mathematics, Computer Science, or related field. 3+ years of SAS programming experience in pharmaceutical or CRO environments. Strong knowledge of clinical trials, statistical methods, and regulatory requirements. Proven experience leading programming projects and mentoring team members. Excellent communication skills and experience working with global teams and clients. Proficient in Microsoft Office and SAS software.
What you’ll do
The Senior Statistical Analyst I will develop and validate complex analysis datasets and TFLs using SAS, while also serving as a project lead programmer. Responsibilities include writing programming specifications, mentoring team members, and ensuring compliance with regulatory standards.
Requirements
Candidates must have a bachelor's degree or higher in a relevant field and at least 3 years of SAS programming experience in pharmaceutical or CRO environments. Strong knowledge of clinical trials and experience in leading programming projects are also required.
Listed skills
- Project management · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- SAS Programming
- Statistical Analysis
- Clinical Trials
- Regulatory Requirements
- Project Management
- Mentoring
- Communication
- Documentation
- Quality Assurance
- ADaM
- TFLs
- Macros
- Technical Guidance
- SOP Compliance
- Microsoft Office
- Team Leadership
Job areas
- Healthcare
- Data & Analytics
- Science & Research
- Technology
- Management & Leadership