Role Summary
Senior Programmer on the Programming team to help expand what’s possible for patients with serious diseases. Provide programming and analytical support to clinical studies, working with Biostatistics, Clinical Operations, Data Management, Project Management, and external vendors.
Responsibilities
- Provide programming support to clinical studies and submissions
- Creation of CDISC compliant SDTM and ADaM datasets using SAS for CSR and ad hoc analyses
- Creation of SAS macros and other utility programs
- Performing statistical analysis, generating analytic reports, tables, figures, and slides in support of clinical study and other reports
- Professional development to enhance knowledge, skills, communication, scientific methodology, operational efficiency, and compliance with policies, regulations, and corporate standards and processes
Qualifications
- Required: Bachelor’s degree and 3+ years of experience in pharmaceutical/biotech
- Required: Solid programming background and advanced SAS programming skills
- Required: Good communication skills (verbal and written)
- Required: Highly organized with strong attention to detail, clarity, accuracy and conciseness
- Required: Ability to interact successfully in a dynamic and culturally diverse workplace
- Preferred: Programming skills or experience with VBA, Python, etc.
- Preferred: Other statistical software knowledge (R, S-Plus, WinBugs, etc.)
Skills
- Strong SAS programming skills
- Analytical and statistical reporting abilities
- Effective communication and collaboration with cross-functional teams
Education
- Bachelor’s degree in a related field
Additional Requirements
- Remote work with occasional travel for team meetings or events; minimal travel expected