SAS Programmer in Clinical Trials

Company Description

We are a company that cares – for our staff, clients, partners, and the quality of our work. Founded in 1995, we are a dynamic, global organization with over 3,000 dedicated individuals working on the forefront of medical science, changing lives and bringing new medicines to those in need.

Position Title: Clinical Data Scientist

Reporting to the Clinical Data Science Manager, the Clinical Data Scientist is a key member of our team at PSI. You will work with clinical trial patient and operational data, develop new data solutions, and establish Risk-based Monitoring systems within the Process Improvement department.

Location: Hybrid work in Milan

• Participate in selecting 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's data platform.
• Program and generate 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

• 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 working with relational databases, data warehousing, data schemas, data modeling, testing, validation, and analysis.
• Full professional proficiency in English and Italian.
• Strong analytical and logical thinking skills.
• Excellent communication and collaboration skills.

Nice to have:

• SAS programming experience with SQL.
• Experience in biostatistics or clinical programming departments.
• Knowledge of CDISC SDTM standards.
• Experience with CluePoints RBM system.
• Knowledge of statistical methods and techniques for data analysis.
• Experience using machine learning techniques and products for testing and validation.

What we offer:

• A quick recruitment process, often completed in 3 meetings.
• Extensive onboarding and mentorship to ensure high-quality work.
• Modern, spacious office in a convenient location, with a friendly and supportive team.
• Permanent employment with a stable, privately owned company.
• Competitive salary, good work-life balance with flexible hours, additional days off, insurance, sports and lunch cards.
• Opportunities for personal and professional growth as we continue to expand.

Take your career to the next level by joining a company that values its people and invests in their success.

Please submit your CV in English.