Statistical Programmer

Veeda Lifesciences is seeking a Statistical Programmer I based in Athens, Greece for its growing international hematology/oncology Clinical Trials program.

This is a full-time job.

Job overview:

The Statistical Programmer I is responsible for providing clinical programming expertise and support to clinical studies across multiple therapeutics areas, as part of the Company’s global Phase I-III program.

Main responsibilities:

• Create and/or review Internal Data Review Models (DRMs) and SDTM mapping specifications, annotated CRFs (aCRFs), datasets, define.xml files, and cSDRG documentation for stakeholder use, including data cleaning, medical review, central monitoring, and adaptive decision-making activities
• Write SAS programs, under senior supervision, to develop ADaM datasets and ADaM TFLs in accordance with CDISC standards and implementation guidelines
• Perform data transfers to external recipients and ensure data integrity throughout the process
• Collaborate closely with Data Management, Biostatistics, and other stakeholders to deliver accurate, high-quality programming outputs
• Support the preparation of regulatory submission packages and ensure compliance with applicable standards and requirements
• Contribute to process improvement initiatives within the department
• Comply with the Company’s Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection

Job Requirements:

• BSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or a related field
• MSc in Statistics, Mathematics, Biostatistics, Data Analysis, Data Science, or a related field is desirable
• At least 2 years of SAS programming experience supporting CDISC-compliant clinical studies within a CRO, pharmaceutical company, or equivalent institution
• Excellent command of English, both oral and written
• Strong knowledge of Base SAS, SAS/STAT, SAS Graph, and SAS Macro Language
• Good understanding of CDISC SDTM standards and requirements
• Excellent statistical programming skills
• Expertise in manipulating, validating, and analyzing SAS datasets
• Strong understanding of FDA submission requirements for clinical trial data
• Hands-on experience working with clinical trial data and data transformation processes
• Excellent analytical and computer skills
• Strong communication and interpersonal skills
• Ability to work effectively in a collaborative and multidisciplinary environment
• Genuine interest in clinical research and drug development
• Strong organizational, problem-solving, and decision-making abilities
• Ability to work according to established SOPs, guidelines, regulations, and ethical principles in daily practice

Join us to be part of a multidisciplinary team of highly skilled scientists and healthcare professionals in the forefront of Clinical Research within a friendly work environment.