¡Activa las notificaciones laborales por email!

SAS Programmer in Clinical Trials

Psi CRO Ag

Madrid

Presencial

EUR 50.000 - 70.000

Jornada completa

Hace 30+ días

Mejora tus posibilidades de llegar a la entrevista

Elabora un currículum adaptado a la vacante para tener más posibilidades de triunfar.

Descripción de la vacante

A leading global organization seeks a Clinical Data Scientist to work with clinical trial data, develop innovative solutions, and establish Risk-based Monitoring systems. The role requires strong analytical skills and proficiency in SAS and SQL. Join a supportive team and enjoy competitive benefits.

Servicios

Life and Medical Insurance
Sports and Lunch Cards
Flexible Working Hours
Additional Days Off

Formación

  • At least 4 years of SAS programming experience in the clinical domain.
  • Minimum 2 years of experience in data engineering.

Responsabilidades

  • Manage complex datasets from multiple sources.
  • Calculate Key Risk Indicators and Quality Tolerance Limits.
  • Communicate data findings effectively to stakeholders.

Conocimientos

Analytical Thinking
Communication
Collaboration

Educación

Degree in Data Science
Degree in Mathematics
Degree in Statistics
Degree in Computer Science

Herramientas

SAS
SQL

Descripción del empleo

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 passionate individuals working at the forefront of medical science, changing lives and delivering new medicines to those in need.

Job Description

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 innovative data solutions, and establish Risk-based Monitoring systems within the Process Improvement department.

  • Participate in selecting the Risk-Based Monitoring (RBM) system and provide relevant training to project teams and / or sponsors.
  • Set up and maintain RBM systems in collaboration 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 across functions to identify study challenges and develop data-driven 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

Must have :

  • A degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent.
  • At least 4 years of SAS programming experience in the clinical / pharmaceutical domain.
  • Minimum 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 Spanish.
  • Strong analytical and logical thinking skills.
  • Excellent communication and collaboration abilities.

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 for data analysis.
  • Experience with machine learning techniques and product testing / validation.

Additional Information

What we offer :

  • A quick recruitment process, typically within 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, flexible working hours, additional days off, and benefits such as life and medical insurance, sports and lunch cards.
  • Opportunities for personal and professional growth as we continue to expand.

Make the right move and elevate your career. Join a company that values its people and invests in their development and success.

J-18808-Ljbffr

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.