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Clinical SAS Programmer

NoyMed CRO
Remote

Quick Apply

Job Details

Full-time | Contract

Qualifications

Data integrity assurance
Research project management
Statistics
Clinical research
Statistics
Qualitative data analysis
Data validation techniques
SAS
English
SAS language
Statistical analysis
Bachelor's degree
Team training
Data quality monitoring
CDISC standards
Organizational skills
Clinical trials
Managing projects
Clinical quality assurance standards
Training & development
Query management
Clinical data analysis
Quantitative research
Software training
Cross-functional communication
Quality data entry
Data extraction
Data analysis software

Full Job Description

Job Summary

NoyMed CRO is on the lookout for experienced Mid-Senior Statistical Programmers to join our innovative team. Your strong communication skills and creative problem-solving mindset will be vital in delivering high-quality statistical programming solutions that drive successful project outcomes. Join us in making a meaningful impact in the world of clinical research!

Responsibilities

Understand and conduct work consistent with GCP, ICH, 21 CFR part 11, internal SOPs and international regulatory requirements
Lead, or perform a leading role in statistical programming activities to maintain project plan, track daily status updates and timelines within the team, ensure budget monitoring and adherence, as well as efficient communication methodology with clients
Interact with the project statistician and guide other programmers participating in a project completion
Responsible for accuracy, traceability, and reproducibility of data, quality, and reliability of deliverables of the project
Develop and validate specifications for SDTM datasets and analysis datasets following SDTM and ADaM Implementation Guides, statistical analysis plans
Develop and validate algorithms and programs to create datasets
Develop complex SAS macros in order to automate and standardize routine processes
Develop, upgrade, and validate the programs to produce Tables, Listings, and Graphs
Act as a mentor and tutor for junior programmers

Skills

SAS (Advanced Macros, PROC SQL, Reporting)
CDISC Standards (SDTM, ADaM)
Regulatory submission support (FDA, EMEA)
TLF development & QC validation
Cross-functional and vendor collaboration

Required Qualifications

At least Bachelor's degree in Computer Science or a related field
5+ years’ of relevant work experience
Excellent English skills
Strong sense of discipline and responsibility
In-depth understanding of data collection, data flow management, data quality, data extraction, and data standards with solid knowledge of CDISC standards for CDASH, SDTM, and ADaM
Experience with multiple programming languages (SAS programming language, R, SQL, or other languages/tools as required, SAS Certification desired), including the creation of data entry and query screens/processes and data quality checks
In-depth knowledge of research processes, clinical operations, and data quality management
Strong attention to detail and demonstrated proficiency in quantitative and qualitative analyses
Ability to manage multiple projects, tasks, and priorities; work independently with minimal supervision and execute tasks to completion without a great deal of direction
Experience in training users in the operation of clinical trial software and tools
Ability to exercise judgment, initiative, and resourcefulness in making decisions in consultation with clinical research personnel, and independently if necessary
Demonstrate strong teamwork and organizational skills; outstanding interpersonal and communication skills

Work Location: Remote

Quick Apply

Refine Your Search

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