Senior Statistical Programmer

Description

Summary: Seeking an experienced Senior Statistical Programmer to support clinical research and data analytics initiatives within the pharmaceutical and healthcare sectors. Highlights: 1. Contribute to impactful clinical projects and drive programming excellence 2. Collaborate with biostatisticians and data management teams 3. Opportunity to mentor junior programmers Urgent Hiring!!! Role: Senior Statistical Programmer We are currently hiring for the position of Senior Statistical Programmer to join a leading organization in the Pharmaceutical and Healthcare industry. Location: Remote (Candidates based in Poland, Romania, Bulgaria, Hungary, Argentina, Brazil, and Armenia are encouraged to apply) Compensation: $20 – $45 per hour Industry: Pharmaceutical \& Healthcare About the Role We are seeking an experienced Senior Statistical Programmer to support clinical research and data analytics initiatives within the pharmaceutical and healthcare sectors. In this role, you will collaborate with biostatisticians, clinical data managers, and cross\-functional teams to deliver high\-quality statistical analyses and ensure compliance with industry standards and regulatory requirements. This position offers the opportunity to contribute to impactful clinical projects, mentor junior programmers, and help drive programming excellence across the organization. Key Responsibilities 1\. Develop and validate SAS programs for the creation of SDTM, ADaM datasets, tables, listings, and figures (TLFs) for clinical trial data. 2\. Collaborate with biostatisticians and data management teams to interpret project requirements and statistical analysis plans. 3\. Perform data manipulation, validation, and statistical analyses using appropriate programming methodologies. 4\. Review and validate programming specifications and outputs to ensure accuracy, quality, and regulatory compliance. 5\. Mentor and support junior statistical programmers, promoting best practices and professional growth. 6\. Contribute to the development and implementation of programming standards and process improvements. 7\. Support regulatory submissions by preparing required documentation and assisting during audits and inspections. Requirements Technical \& Professional Qualifications Bachelor's degree in Statistics, Biostatistics, Mathematics, or a related discipline (Master's degree preferred). Minimum of 5 years' experience in statistical programming within pharmaceutical, biotechnology, or clinical research environments. Advanced proficiency in SAS programming; experience with R is highly desirable. Strong knowledge of clinical trial design, CDISC standards (SDTM/ADaM), and regulatory requirements. Experience with data management processes, quality control, and data validation techniques. Excellent analytical and problem\-solving skills with strong attention to detail. Interested candidates are encouraged to apply to **precious.omobobola@recruitifyhr.com**. Only shortlisted applicants will be contacted. Job Type: Full\-time Application Question(s): * How soon can you resume? * How many years of experience in statistical programming within the pharmaceutical or clinical research industry do you have? Work Location: Remote