SAS Programmer in Clinical Trials

TN United Kingdom; Oxford; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Clinical Data Scientist to enhance their clinical trial processes. This role involves working with patient and operational data, developing innovative data solutions, and setting up Risk-Based Monitoring systems. You will collaborate with various teams to analyze complex datasets, communicate findings effectively, and contribute to the development of software products and quality systems. The company offers a permanent work contract, competitive salary, and opportunities for personal and professional growth in a supportive environment. Join us to elevate your career in a dynamic and stable company.

Benefits

Fast recruitment process

Extensive onboarding and mentorship

Modern office

Competitive salary

Flexible hours

Additional days off

Insurance

Sports and lunch cards

Opportunities for growth

Qualifications

• 4+ years of SAS programming experience in Clinical/Pharmaceutical domain.
• Experience in data engineering with relational databases and data warehousing.

Responsibilities

• Manage complex datasets and program data listings for Clinical Data Reviewers.
• Collaborate to identify study challenges and develop data solutions.

Skills

SAS Programming

Data Engineering

Analytical Skills

Communication Skills

Education

Degree in Data Science

Degree in Mathematics

Degree in Statistics

Degree in Computer Science

Tools

SQL

CluePoints RBM System

Job description

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SAS Programmer in Clinical Trials, Oxford

Client: PSI CRO

Location: Oxford, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: 047bb6f20b2f

Job Views: 3

Posted: 08.05.2025

Expiry Date: 22.06.2025

Job Description

The position is titled Clinical Data Scientist, reporting to the Clinical Data Science Manager. You will work with clinical trial patient and operational data, develop data solutions, and set up Risk-based Monitoring systems in the Process Improvement department.

Responsibilities include:

• Participate in selecting the Risk-Based Monitoring (RBM) system and provide training to the project team and/or Sponsor
• Set up and maintain RBM systems, collaborating with the Central Monitoring Manager
• Manage complex datasets from multiple sources, including data extraction, transformation, and loading into PSI data platform
• Program and produce data listings, tables, and figures for Clinical Data Reviewers and Central Monitoring Managers
• Calculate Key Risk Indicators and Quality Tolerance Limits, applying advanced analytical techniques to identify data trends for Centralized Monitoring
• Collaborate cross-functionally to identify study challenges and develop data solutions using advanced analytics
• Communicate data findings and solutions effectively to stakeholders
• Contribute to the development of databases, software products, processes, and Quality System Documents for Centralized Monitoring

Qualifications

Must have:

• Degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent
• Minimum 4 years of SAS programming experience in the Clinical/Pharmaceutical domain
• At least 2 years of experience in data engineering, including relational databases, data warehousing, data schemas, data modeling, testing, validation, and analysis
• Full professional proficiency in English
• Strong analytical and logical thinking skills
• Good communication and collaboration skills

Nice to have:

• SAS programming experience with SQL
• Experience in Biostatistics or Clinical Programming Department
• Knowledge of CDISC SDTM
• Experience with CluePoints RBM system
• Knowledge of statistical methods and techniques for data analysis
• Experience with Machine Learning techniques and products testing and validation

Additional Information

What we offer:

• Fast recruitment process—up to 3 meetings
• Extensive onboarding and mentorship
• Modern, spacious office in a convenient location with a friendly team
• Permanent work contract in a stable, privately owned company
• Competitive salary, flexible hours, additional days off, insurance, sports and lunch cards
• Opportunities for personal and professional growth

Join us to elevate your career and be part of a company that invests in its people. Please submit your CV in English.