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Senior SAS Programmer

P-Product, a leading and innovative company in Software development and Data solutions, is looking for an experienced Senior SAS Programmer to join our dynamic team and contribute programming support to the statistics and programming department across a wide range of projects, clients and therapeutic areas. You will have a vital role in helping our clinical trials and drug development processes succeed.


Key Responsibilities:

● Perform SAS programming to create, validate, and maintain analysis datasets, tables, listings and figures for clinical trials and reports according to study protocol and statistical analysis plans.

● Lead the clinical trials flow development from study protocols development to final data analysis, documentation and provisioning the datasets for regulatory submission.

● Adhere to GCP, ICH, and other regulatory guidelines for pharmaceutical data reporting, managerial, scientific and technical tasks.

● Integrate data from different sources and ensure that the datasets are consistent and reliable.

● Collaborate closely with various teams and professionals, such as researchers, data analysts, biostatisticians, data managers and other key stakeholders, to ensure data quality and integrity and observance of regulatory, industry and company standards.

● Coach and mentor junior SAS programmers and create a learning and growth environment.


Required Knowledge and Skills:

● BSc, MSc or PhD in Statistics, Mathematics, Computer Science, or related field.

● 5+ years of extensive programming experience in SAS in a clinical trial environment.

● Extended experience with SAS/BASE, SAS/MACRO, SAS/GRAPH and SAS/STAT.

● Professional knowledge and experience with CDISC clinical data standards, such as CDISC, ADaM and SDTM.

● Proven ability to develop specifications for datasets and outputs of any complexity according to the requirements, as well as independently write SAS programming code and validation scripts in a good quality manner.

● Proven statistical expertise, especially in efficacy outputs programming.

● Excellent knowledge of drug development processes and regulatory submission requirements.

● Exceptional analytical and problem-solving skills, strong organizational and communications skills, high attention to detail and commitment to accuracy, proactive mindset and capability to work independently as well as in a team environment.


Will Be a Plus:

● SAS certification.

● Team leading and mentoring experience

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