Sr. Programmer Clinical Data Programming (CDP)(Remote)
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
Apply Now
Apply Now
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
Apply Now
Apply Now