We are seeking an experienced Senior Statistical 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).
*Key Responsibilities:*
• Lead programming activities for assigned clinical studies, ensuring adherence to study protocols, statistical analysis plans (SAPs), and regulatory requirements.
• Coordinate the delivery of study specific programming deliverables from a assigned team which my be local or global. Ensure key members of the team are effectively informed about study decisions, timelines and customer expectations.
• 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.
*Qualifications:*
• Bachelors degree in Computer Science, Statistics, Mathematics, or a related field;.
• Minimum of 5 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.
Employee requirements
Education
University education (Bachelor's degree) University education (Master's degree) Postgraduate (Doctorate)
Specialisation, field
Computer Science, Statistics, Mathematics, or a related field
Language and language level
English - Upper intermediate (B2)
Other knowledge
SAS - advanced
Number of years of experience
5
Experience in the position/sector
IT
Personality requirements and skills
The most important SAS modules are in this role- SDTM, AdaM, TFL
We prefer candidate only from pharma industry
Information about the selection process
The number of job openings
1
A brief description of your client
Client is a dynamic global provider of outsourced development in the pharmaceutical industry dedicated to helping our clients accelerate the development of drugs and devices that save lives and improve quality of life.
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