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Clinical Programmer

The Steely Group

Remote, CA(remote)

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JOB DETAILS
SKILLS
Analysis Skills, Best Practices, Biotech and Pharmaceutical, Case Report Form (CRF), Clinical Data Interchange Standards Consortium (CDISC), Communication Skills, Computer Programming, Computer Science, Cross-Functional, Data Cleaning, Data Management, Data Mapping, Data Processing, Data Quality, Data Sets, Data Visualization, Debugging Skills, Delivery Management, Documentation, Electronic Data Capture (EDC), Epidemiology, Industry Standards, Interpersonal Skills, Maintain Compliance, Mathematics, Problem Solving Skills, Process Analysis, Process Improvement, Programming Methodologies, Project/Program Management, Quality Control, Reconciliation, Regulatory Reports, SQL (Structured Query Language), Statistical Analysis System (SAS), Statistical Programming Languages, Statistics, Team Lead/Manager, Time Management, Validation Documentation, Validation Testing
LOCATION
Remote, CA
POSTED
4 days ago
Our client is looking to add a Clinical Programmer to their team on a contract basis.

Responsibilities:
  • Develop and validate SAS programs for data review, cleaning, and reconciliation listings
  • Program listings, tables, profiles, figures, and standard datasets following best practices and specifications
  • Generate validation and quality check documentation
  • Execute existing SAS programs and macros, including debugging and error resolution
  • Identify and implement process and programming improvements
  • Perform EDC user administration using templates and standard practices
  • Develop and apply SAS macros and SQL to improve programming efficiency
  • Perform data mapping between multiple data sources and standard outputs using annotated CRFs and industry standards
  • Conduct data quality checks and maintain supporting documentation
  • Develop data visualization packages based on requirements and specifications
  • Analyze, process, and execute data reconciliation and integration requirements
  • Provide input into complex report and listing specifications
  • Manage programming deliverables for assigned studies, tasks, and projects
  • Assist with resolving data issues with data providers
  • Perform quality assessments on internally and externally developed programs and data packages
  • Support routine programming, validation, and documentation activities
  • Collaborate with data managers and cross functional study teams
  • Assist with statistical programming activities as needed
  • Perform quality control checks on programmed data and reports to ensure regulatory compliance
  • Identify and resolve data quality and consistency issues
  • Maintain detailed documentation for programming activities, code development, and validation processes

Qualifications: 
  • Proven experience in Pharma, Biotech, and SAS Programming
  • Bachelor’s degree or higher in scientific, biological, statistical, computer science, or related field
  • Master’s degree in Statistics, Mathematics, or Epidemiology preferred
  • Strong analytical, problem solving, organizational, and time management skills
  • Excellent interpersonal and communication skills
  • Proficiency in programming, including SAS certification preferred
  • Experience with academic or industry projects demonstrating programming techniques and platforms is a plus
  • Fast learner with the ability to adapt to changing environments and priorities
  • Demonstrates high integrity and trustworthiness
  • Strong sense of personal accountability and ability to work independently on challenging assignments
  • General knowledge of industry standards and best practices including CDISC, CDASH, SDTM, and data standardization

About the Company

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The Steely Group

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