SAS Programmer in Clinical Trials

PSI
Municipality of Madrid, Spain
yesterday

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Working hours
Regular working hours
Languages
English, Spanish
Experience level
Intermediate

Job location

Municipality of Madrid, Spain

Tech stack

Data analysis
Big Data
Clinical Data Repository
Databases
Information Engineering
Data Mining
Data Stores
Data Systems
Data Warehousing
Database Schema
Monitoring of Systems
Machine Learning
Operational Data Store
SAS (Software)
SQL Databases
Information Technology

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

  • 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

Requirements

  • 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 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

Benefits & conditions

  • 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.

About the company

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.

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