Company 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 Process Improvement department.

Hybrid work in Milan

Participate in 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 Clinical/Pharmaceutical domain
At least 2 years of experience in data engineering area 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 and Italian
Strong analytical and logical thinking
Communication and collaboration skills

Nice to have:

SAS programming experience with SQL programming
SAS programming experience in Biostatistics Department 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 technics and products testing and validation

Additional Information

What we offer:

We value your time so the recruitment process is as quick as 3 meetings
We'll prepare you to do your job at highest quality level with our extensive onboarding and mentorship program
You'll have excellent working conditions - spacious and modern office in convenient location, and friendly, supportive team who love to hang out together
You'll have permanent work agreement at a stable, privately owned company
We care about our employees - aside from competitive salary, you'll have good work-life balance with flexible working hours and additional days off, life and medical insurance, sports card, lunch card
We're constantly growing which means opportunities for personal and professional growth

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

Please submit your CV in English

Jobs in Milano

SAS Programmer in Clinical Trials