Clinical Statistical Programmer

Clinical Statistical Programmer

NoyMed

Remote, Europe

NoyMed CRO is on the lookout for experienced Mid-Senior Statistical Programmers to join our innovative team. Your strong communication skills and creative problem-solving mindset will be vital in delivering high-quality statistical programming solutions that drive successful project outcomes. Join us in making a meaningful impact in the world of clinical research!

Responsibilities

• Understand and conduct work consistent with GCP, ICH, 21 CFR Part 11, internal SOPs, and international regulatory requirements;
• Interact with the project statistician and guide other programmers participating in a project completion;
• Responsible for the accuracy, traceability, and reproducibility of data, quality, and reliability of deliverables of the project;
• Develop and validate specifications for SDTM and ADaM datasets, following the SDTM and ADaM Implementation Guides and statistical analysis plans;
• Develop and validate algorithms and programs to create datasets;
• Develop complex SAS macros in order to automate and standardize routine processes;
• Develop, upgrade, and validate the programs to produce Tables, Listings, and Graphs (TLFs);
• Lead, or perform a leading role in statistical programming activities to maintain the project plan, track daily status updates and timelines within the team, ensure budget monitoring and adherence, as well as efficient communication methodology with clients;
• Act as a mentor and tutor for junior programmers.

Required Qualifications

• At least a Bachelor's degree in Computer Science or a related field;
• 4+ years of relevant work experience;
• Excellent English skills;
• Strong sense of discipline and responsibility;
• In-depth understanding of data collection, data flow management, data quality, data extraction, and data standards, with solid knowledge of CDISC standards;
• Experience with multiple programming languages (SAS programming language, SQL, as required; R, or other languages/tools; SAS Certification desired);
• In-depth knowledge of research processes, clinical operations, and data quality management;
• Strong attention to detail and demonstrated proficiency in quantitative and qualitative analyses;
• Ability to manage multiple projects, tasks, and priorities; work independently with minimal supervision and execute tasks to completion without a great deal of direction;
• Experience in training users in the operation of clinical trial software and tools;
• Ability to exercise judgment, initiative, and resourcefulness in making decisions in consultation with clinical research personnel, and independently if necessary;
• Demonstrate strong teamwork and organizational skills; outstanding interpersonal and communication skills.

Application instructions

If you are interested in this position, please apply now by sending your CV to us via career@noymed.com, mentioning “SAS Programmer” in the Subject Line of your e-mail.

Please note that only shortlisted candidates will be contacted for the interview.