SAS Programmer in Clinical Trials

PSI CRO; Madrid; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading global company is seeking a Clinical Data Scientist for its Madrid office, focusing on clinical trials data solutions and Risk-Based Monitoring systems. The role offers a collaborative environment and requires strong analytical skills and SAS programming experience. Competitive salary and benefits with opportunities for professional growth are offered.

Servicios

Flexible working hours

Life and medical insurance

Sports and lunch cards

Formación

• 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 and Spanish.

Responsabilidades

• Participate in selection of Risk-Based Monitoring systems.
• Manage complex datasets and program data listings.
• Collaborate cross-functionally for study challenges.

Conocimientos

SAS programming

Data analysis

Analytical thinking

Communication

Collaboration

Educación

Degree in Data Science, Mathematics, Statistics or equivalent

Herramientas

SQL

Machine Learning

Descripción del empleo

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 than3000 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 Madrid

• Participatein selection of the Risk-Based Monitoring (RBM) system and providerelevant 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 Spanish
• Strong analytical and logical thinking
• Communication and collaboration skills

Nice to have:

• SAS programming experience with SQL programming
• SAS programming experience in BiostatisticsDepartmentor Clinical Programming Department
• Knowledgeof CDISC SDTM
• Experience with CluePoints RBM system
• Knowledge of statistical methodsand techniques for analyzing data
• Experienceusing Machine Learning technics andproducts 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 havepermanent 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 meansopportunities 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