We are seeking an experienced Senior SAS Programmer to join our team. The ideal candidate will have proven expertise in SAS programming, with a strong ability to lead programming efforts for clinical studies and produce high-quality Tables, Listings, and Figures (TLFs).
Responsibilities:
- Lead SAS programming activities for clinical studies, ensuring adherence to study protocols, statistical analysis plans (SAPs), and regulatory requirements
- Develop, validate, and maintain SAS programs to generate analysis datasets, TLFs, and other clinical trial deliverables
- Collaborate closely with cross-functional teams including statisticians, data managers, and clinical operations to ensure timely and accurate deliverables
- Provide technical guidance and mentorship to junior programmers, ensuring adherence to programming standards and best practices
- Participate in study team meetings, contributing SAS programming expertise to study design and analysis strategies
- Contribute to the development and implementation of departmental programming standards and processes to optimize efficiency and ensure quality
- Ensure compliance with regulatory guidelines (e.g., FDA, ICH) and company SOPs throughout all programming activities
Requirements:
- Bachelor's degree in Computer Science, Statistics, Mathematics, or a related field; advanced degree preferred
- Minimum 7 years of hands-on experience in SAS programming within the pharmaceutical, biotechnology, or clinical research industry
- Proficiency in SAS/Base, SAS/STAT, SAS/Macro, and other relevant SAS modules
- Demonstrated experience in leading SAS programming efforts for clinical studies, including complex TLFs
- Strong understanding of CDISC standards (e.g., SDTM, ADaM) and their application in clinical trials
- Excellent problem-solving skills, attention to detail, and ability to work effectively in a team environment
- Proven ability to effectively communicate technical concepts to non-technical stakeholders
- Experience with submission deliverables and familiarity with regulatory requirements (e.g., FDA, EMA) preferred
- Prior experience in mentoring junior programmers and leading programming teams is desirable
Our offer:
- Workplace: 100% remote
- MultiSport Plus
- Group insurance
- Medicover Premium
- e-learning platform