Job Description
ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of their clients. ClinChoice is a global full-service CRO with a focus on quality, professional development, and a supportive culture. This client-facing role requires a confident individual capable of working independently and establishing trust with the client's team.Role involves:
- Participating in CRF design, database review, and data management planning.
- Producing data listings, summary tables, and graphics for analyses.
- Integrating data across studies.
- Testing, documenting, reviewing, and validating programs.
- Coordinating data transfer and programming standards with CROs and vendors.
- Validating analysis datasets and TFLs from vendors.
- Collaborating with Biometrics functions for data analysis activities.
- Executing ad-hoc requests, manuscripts, posters, and presentations.
Requirements:
- Minimum of 10 years of SAS programming experience in the pharmaceutical or biotechnology industry with a BA/BS in computer science, statistics, or math, or MA/MS with 8 years of experience.
- Expertise in SAS programming language, report generation, and programming validation standards.
- Experience with CDISC data standards.
- Experience as a senior statistical programmer in a pharmaceutical or CRO within an FDA-regulated environment.
- Experience with Clinical Study Reports and NDA submissions.
- Ability to manage multiple tasks and meet deadlines.
- Excellent verbal, written, and interpersonal skills for cross-functional teamwork.
Role offers:
- Opportunity to work directly for a single sponsor with the security of a global CRO.
- Professional development and a supportive culture.
- Remote work opportunity.