Clinical Data Analyst Lead
4 days ago
Job Description:
The Principal Statistical Programmer will lead and support all programming activities per the project strategies, working independently to implement and drive programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis.
This role may involve leading programming support within multiple studies/projects in various study activities, ensuring timely and high-quality programming deliverables in assigned projects and areas. Developing and maintaining programming documentation and specifications following programming standards and processes is a key responsibility.
Key Responsibilities:
- Lead programming support within multiple studies/projects
- Develop and maintain programming documentation and specifications
- Work closely with internal partnering functions, collaborators, and external functional service providers
Requirements:
- Proficiency in SAS programming skills in a clinical data environment with excellent analytical skills
- Good knowledge of pharmaceutical clinical development
- SAS (Base, Stat, Macro, graph) certificates are a plus
Preferred Qualifications:
- MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline
- 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical, or health-related industry
Estimated Salary: $120,000 - $180,000 per year
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