SAS Programmer in Clinical Trials

PSI CRO AG; Oxford; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading company in the Clinical Research Organization sector is seeking a Clinical Data Scientist to work on clinical trials. The role encompasses data management, advanced analytics, and collaboration with multiple stakeholders to enhance data-driven decision-making. The ideal candidate will have a strong background in data science with SAS programming expertise.

Benefits

Permanent work agreement

Competitive salary

Life and medical insurance

Sports card

Lunch card

Excellent working conditions

Qualifications

• Minimum 4 years of SAS programming experience in Clinical/Pharmaceutical domain.
• At least 2 years of experience in data engineering.
• Full professional proficiency in English.

Responsibilities

• Manage complex datasets from multiple sources, including data extraction and transformation.
• Set up and maintain Risk-Based Monitoring systems.
• Calculate Key Risk Indicators and Quality Tolerance Limits.

Skills

Analytical thinking

Collaboration

Communication

Education

Degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent

Tools

SAS

SQL

Job description

We are the company that cares – for our staff, for our clients, for our partners, and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated, and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Actual position's title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is an integral part of our team here at PSI. You will work with clinical trials patient and operational data, develop new data solutions, and set up Risk-based Monitoring systems in the Process Improvement department.

• Participate in the selection of the Risk-Based Monitoring (RBM) system and provide relevant 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 to stakeholders effectively
• 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 one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling, testing, validation, and analysis
• Full professional proficiency in English
• Strong analytical and logical thinking
• Excellent communication and collaboration skills

Nice to have:

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

Additional Information

What we offer:

• We value your time, so the recruitment process is as quick as 3 meetings
• Extensive onboarding and mentorship programs to prepare you for your role
• Excellent working conditions – spacious, modern office in a convenient location, with a friendly, supportive team
• Permanent work agreement at a stable, privately owned company
• Competitive salary, good work-life balance with flexible hours, additional days off, life and medical insurance, sports card, lunch card
• Opportunities for personal and professional growth as we continue to expand

Make the right call and take your career to a whole new level. Join a company that focuses on its people and invests in their professional development and success.