Job Description
About the position
- Responsibilities
- Build SAS datasets from clinical databases and external data sources.
- Develop SAS macros, templates, and utilities for data cleaning and reporting.
- Utilize SDTM guidelines to build datasets.
- Communicate with internal teams to create deliverables for clients.
- Write SAS programs to generate tables, listings, and figures datasets.
- Act as the SAS Subject Matter Expert (SME) in collaboration with Clinical Data Sciences members on various projects.
- Participate in identifying and creating edit checks per the data transfer plan.
- Create and provide study-specific reports using SAS.
- Monitor data transfers for ongoing trials.
- Requirements
- Bachelor's degree required; advanced degree preferred.
- 7-10 years of SAS and/or ETL programming experience in a business environment required.
- 5 years of SAS Data Programming experience in Clinical trials strongly recommended.
- Experience with electronic Clinical Database Systems is required.
- Knowledge of GCP is essential.
- Detail-oriented with a track record of problem-solving.
- Good verbal and written communication skills.
- Ability to quality check all data deliverables.
- Ability to create presentations and interpret data for clients.
- Knowledge of Microsoft Excel required.
- Knowledge of R or Power BI is a plus.
- Nice-to-haves
- Experience with electronic reporting applications preferred.
- Benefits
- Comprehensive Benefits package - Health, Dental, Vision, Life Disability, 401k with match, and flexible spending accounts
- Employee Assistance Programs and additional work/life resources
- Referral Bonuses and Tuition Reimbursement
- Paid time off including holidays, vacation, and sick time
- Opportunities for career development with on-the-job training, certification assistance and continuing education reimbursement
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