SAS Programmer in Clinical Trials

PSI CRO AG; Madrid; Presencial; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

A global leader in clinical research, PSI CRO AG, is seeking a Clinical Data Scientist to work on clinical trials data. The role involves developing data solutions, managing datasets, and collaborating across teams. Candidates should possess strong analytical skills and a degree in a relevant field, along with proficiency in SAS and SQL. PSI offers a supportive work environment, competitive salary, and opportunities for professional growth.

Servicios

Flexible hours

Life and medical insurance

Sports card

Lunch card

Extensive onboarding and mentorship programs

Formación

• Minimum 4 years of SAS programming experience in the Clinical/Pharmaceutical domain.
• At least 2 years of experience in data engineering.
• Full professional proficiency in English and Spanish.

Responsabilidades

• Participate in the selection and setup of Risk-Based Monitoring systems.
• Manage complex datasets and perform data analysis.
• Communicate data findings effectively to stakeholders.

Conocimientos

Analytical skills

Logical thinking

Communication

Collaboration

Educación

Degree in Data Science, Mathematics, Statistics, Computer Science or equivalent

Herramientas

SAS

SQL

Descripción del empleo

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 the Process Improvement department.

1. Participate in the selection of the Risk-Based Monitoring (RBM) system and provide relevant training to the project team and/or Sponsor.
2. Set up and maintain RBM systems, collaborating with the Central Monitoring Manager.
3. Manage complex datasets from multiple sources, including data extraction, transformation, and loading into PSI data platform.
4. Program and produce data listings, tables, and figures for Clinical Data Reviewers and Central Monitoring Managers.
5. Calculate Key Risk Indicators and Quality Tolerance Limits, applying advanced analytical techniques to identify data trends for Centralized Monitoring.
6. Collaborate cross-functionally to identify study challenges and develop data solutions using advanced analytics.
7. Communicate data findings and solutions to stakeholders effectively.
8. Contribute to the development of databases, software products, processes, and Quality System Documents for Centralized Monitoring.

Qualifications

Must have:

1. Degree in Data Science, Mathematics, Statistics, Computer Science, or equivalent.
2. Minimum 4 years of SAS programming experience in the Clinical/Pharmaceutical domain.
3. At least 2 years of experience in data engineering, including one or more of the following: relationship databases, data warehousing, data schemas, data stores, data modeling, testing, validation, and analysis.
4. Full professional proficiency in English and Spanish.
5. Strong analytical and logical thinking skills.
6. Excellent communication and collaboration skills.

Nice to have:

1. SAS programming experience with SQL programming.
2. SAS programming experience in Biostatistics or Clinical Programming Departments.
3. Knowledge of CDISC SDTM.
4. Experience with CluePoints RBM system.
5. Knowledge of statistical methods and techniques for analyzing data.
6. Experience using Machine Learning techniques and products testing and validation.

Additional Information

What we offer:

1. A quick recruitment process, often completed in 3 meetings.
2. Extensive onboarding and mentorship programs to ensure high-quality job performance.
3. Excellent working conditions — spacious, modern office in a convenient location, with a friendly, supportive team.
4. Permanent work agreement at a stable, privately owned company.
5. Competitive salary, good work-life balance with flexible hours and additional days off, life and medical insurance, sports card, and lunch card.
6. Opportunities for personal and professional growth as the company continues to expand.

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