Statistical Programmer

About Our Client:Everest Clinical Research is a contract research organization (CRO) specializing in clinical research services for the pharmaceutical, biotechnology, and medical device industries worldwide. Established as an independent CRO since 2004, the organization has a strong foundation in statistical and data management and has expanded into a full-service CRO. With headquarters in Canada and the USA and offices in Asia and Europe, the company is recognized for its high-quality deliverables, customer service, and flexibility, supporting advanced drug, biologic, and device development.About the Opportunity:The STATISTICAL PROGRAMMER role is designed to support clinical research projects by developing and validating datasets and statistical reports based on study protocols and regulatory guidelines. This position contributes to the integrity and quality of clinical trial data, supporting the analysis and reporting that drive clinical and regulatory decisions. The role can be performed on-site or remotely within the USA and plays a key part in maintaining compliance and delivering accurate statistical programming services.Responsibilities:Develop and review dataset specifications, annotated case report forms, and related documentation per statistical analysis plans and industry standards.Program and validate SDTM and ADaM datasets, perform conformance checks, and resolve any issues.Develop SAS programs to generate and validate statistical outputs and reports.Support clinical study reporting, data integration, and regulatory safety reporting needs.Develop SAS programs for database integrity checks and collaborate with data managers on data cleaning.Reconcile CRF and non-CRF data, perform data integrity checks, and generate data listings and summaries.Produce patient profiles to support case review activities.Document programming and data processes following company SOPs and maintain audit readiness.Maintain knowledge of industry standards, regulatory requirements, and sponsor-specific needs.Comply with required training and provide expertise in programming and system administration as needed.Requirements:Master's degree or higher in statistics, biostatistics, or a related quantitative field.Minimum two years of clinical trial statistical programming experience.Proficiency in SAS, R, SQL, and Excel.Ability to pass a SAS-based assessment test.Eligible to work remotely from locations within the USA.Pay Range and Compensation Package:Estimated salary range: $80,000 to $116,000.Benefits & Perks:Medical, dental, and vision insurance coverage.Life and AD&D insurance.Short- and long-term disability insurance.Tuition reimbursement and fitness reimbursement programs.Employee assistance program (EAP).401(k) retirement plan.Generous paid time off and sick leave.Opportunity to earn a performance-based bonus.Equal Opportunity Statement: Our client is an equal opportunity employer. They celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, or national origin.Note:RemoteHunter is a recruitment partner of this role. Please note that all employment decisions, including candidate assessment, interviews, hiring, compensation, and employment terms, are made exclusively by the hiring employer.