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SAS Programmer in Clinical Trials

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 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

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 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

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Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About SAS Programmer in Clinical Trials, PSI CRO

Are you ready to make a difference in the world of clinical trials? Join our dynamic team at PSI as a SAS Programmer in Clinical Trials in vibrant Madrid, Spain! Here at PSI, we pride ourselves on being a company that truly cares for our staff, clients, and partners. You'll be part of a global team of over 3000 passionate individuals, all dedicated to improving lives through innovative medical solutions. In this role, you'll report directly to the Clinical Data Science Manager and play an essential part in analyzing clinical trial patient data. As a SAS Programmer, you'll manage complex datasets, develop new data solutions, and set up Risk-based Monitoring systems. You'll be collaborating with various teams, creating data listings, tables, and figures, all while applying advanced analytical techniques to ensure the highest quality data monitoring. With at least four years of SAS programming experience in the Clinical or Pharmaceutical domains, and at least two years in data engineering, you have the skills to drive impactful decisions. In addition to professional growth opportunities, we offer flexible working hours, a supportive team environment, and a commitment to your well-being with excellent benefits. If you’re a strong communicator who’s excited to tackle challenges with data and innovation, we can’t wait to meet you. Join us at PSI and let’s work together for a healthier tomorrow!

Frequently Asked Questions (FAQs) for SAS Programmer in Clinical Trials Role at PSI CRO
What are the primary responsibilities of a SAS Programmer at PSI in Clinical Trials?

As a SAS Programmer at PSI, your main responsibilities will include managing complex datasets from various sources, programming and producing data listings and tables for Clinical Data Reviewers, and setting up Risk-based Monitoring systems. You'll collaborate cross-functionally to identify study challenges and employ advanced analytics to find effective solutions, while also communicating your findings clearly to key stakeholders.

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What qualifications do I need to apply for the SAS Programmer position at PSI?

To be considered for the SAS Programmer role at PSI, you should have a degree in Data Science, Mathematics, Statistics, or Computer Science. You’ll need at least four years of SAS programming experience in the clinical or pharmaceutical domain, along with a minimum of two years in data engineering. Proficiency in both English and Spanish is essential, alongside strong analytical skills.

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What programming skills are preferred for a SAS Programmer at PSI?

For the SAS Programmer position at PSI, familiarity with SAS programming is mandatory, but experience with SQL programming is highly advantageous. Knowledge of CDISC SDTM standards and experience with the CluePoints Risk-Based Monitoring system are also valuable assets that can enhance your application.

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What opportunities for professional growth does PSI offer to its SAS Programmers?

At PSI, we’re committed to the professional development of our employees. As a SAS Programmer, you will benefit from an extensive onboarding and mentorship program that empowers you to excel in your role. Additionally, our constant growth results in numerous opportunities for personal and professional advancement in your career path.

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What benefits can I expect when working as a SAS Programmer at PSI?

Working at PSI as a SAS Programmer comes with excellent benefits, including a competitive salary, flexible working hours, a supportive team environment, and health insurance coverage. You’ll also enjoy additional perks like a sports card, lunch card, and opportunities for a healthy work-life balance, ensuring both your professional and personal needs are met.

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Common Interview Questions for SAS Programmer in Clinical Trials
Can you explain your experience with SAS programming in clinical trials?

In your response, detail specific projects where you utilized SAS programming. Highlight the complexity of the data sets you handled and any methodologies you employed. Showcase any outcomes you improved through your programming skills to demonstrate your impact on the trials.

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How do you manage and clean large datasets in SAS?

Discuss your methodical approach to data management. Include techniques for data cleaning, such as identifying outliers and ensuring accuracy. Reference any tools or SAS-specific functions you use, and highlight the importance of data integrity in clinical trials.

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What experience do you have with Risk-Based Monitoring systems?

Share any past roles where you contributed to Risk-Based Monitoring systems. Describe your involvement in selecting tools and training teams. This will show your comprehensive understanding of how RBM compliments clinical data management.

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How do you handle tight deadlines while working on clinical datasets?

Acknowledge the importance of prioritizing tasks and effective time management. Share strategies you’ve employed in previous roles to stay on track, such as breaking projects into manageable parts and using software tools for efficient tracking.

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Can you give an example of how you used advanced analytics to solve a data-related problem?

Provide a specific example of a challenge you faced and the advanced analytical techniques you applied to arrive at a solution. Highlight the outcome, emphasizing how your analytical skills contributed to improving the study or project.

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What statistical methods are you familiar with that are applicable to clinical data?

Discuss various statistical methods such as regression analysis, survival analysis, and hypothesis testing that you have experience with. Be prepared to provide examples of how you applied these techniques in real-world scenarios.

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How do you ensure communication with cross-functional teams during a project?

Emphasize the importance of open communication and regular check-ins. Mention tools you use for collaboration and how you tailor your communication style to suit different audiences to ensure all stakeholders are informed and engaged.

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What do you think is the most critical skill for a SAS Programmer in Clinical Trials?

Highlight technical proficiency in SAS programming, but also the significance of problem-solving abilities and attention to detail. Stress that the combination of these skills leads to effective and precise data management, crucial for the success of clinical trials.

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How do you stay updated with the latest trends in clinical data science and analytics?

Mention specific resources you follow, such as industry blogs, conferences, or webinars. Discuss your commitment to continuous learning and any formal training or certifications you might seek to enhance your skills in clinical data science.

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Why do you want to work as a SAS Programmer at PSI?

Articulate your passion for contributing to the healthcare sector and how PSI's values align with your professional goals. Visit specific aspects of the company that excite you, such as its commitment to employee development and the impactful work being done in clinical trials.

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Full-time, hybrid
DATE POSTED
March 23, 2025

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