Senior Statistical Programmer (Oncology)

IQVIA; Durham (NC); On-site; USD 88,000 - 221,000; Full time

Job summary

IQVIA is seeking a SAS programmer in the United States (Durham, NC area) to perform statistical programming for clinical data in accordance with ICH guidelines and SOPs. You will develop analysis datasets per CDISC standards, create tables and graphs, and support SAP preparation with minimal supervision.

The role requires 4–8 years of SAS experience in pharma, strong attention to detail, and the ability to manage multiple tasks under tight timelines.

Qualifications

• BA/BS in math, statistics, CS or health field, or equivalent experience.
• 4–8 years of SAS programming in pharma.
• Strong SAS skills and meticulous attention to detail.
• Knowledge of regulatory guidelines including electronic submission standards.
• Strong organizational, communication, and leadership skills.
• Ability to work under tight deadlines and handle multiple tasks.

Responsibilities

• Conduct statistical programming on clinical data using SAS.
• Ensure programs, outputs, and docs follow ICH guidelines and SOPs.
• Create analysis datasets per CDISC standards and SAP.
• Produce summary tables, graphs, and listings; perform adhoc analyses.
• Validate programs and outputs created by colleagues.
• Assist in SAP preparation and TLF shell review.
• Run CDISC validation (OpenCDISC) to ensure ADaM CDISC compliance.
• Learn and implement Incyte SAS macros for efficiency.
• Program independently for studies with minimal supervision.
• Check validation summary reports for errors and proper docs.
• Review CDISC validation output for each study.

Skills

SAS programming

CDISC standards

Regulatory knowledge

Leadership

Time management

Communication

Attention to detail

Education

BA/BS in math, statistics, CS or health

Tools

SAS

OpenCDISC

Job description

Essential Functions Of The Job (Key Responsibilities)

• Conduct statistical programming work of clinical data using SAS Software.
• Ensure that all programs, outputs and documentation are consistent with ICH guidelines and are conducted in compliance with company SOPs.
• Generate analysis datasets according to CDISC standard and SAP.
• Implement analysis methods according to SAP, and produce summary tables, graphs and data listings using SAS; Conduct adhoc analyses.
• Validate programs and associated results produced by other programming colleagues.
• Participate in TLF shell preparation and review, and assist statistician for SAP preparation.
• Run CDISC validation programs e.g. OpenCDISC reports to ensure ADaM datasets are CDISC compliant.
• Learn, and implement Incyte standard SAS macros for efficient analyses of clinical data supervised by Lead programmers.
• Work independently to program for individual studies with minimum supervision.
• Check that the validation summary reports are clean of errors and warnings, and show proper documentation of SAS programs.
• Review individual study CDISC validation output.

Qualifications (Minimal acceptable level of education, work experience, and competency)

• BA/BS degree in mathematics, statistics, computer science or health related field. Or equivalent experience
• 4 – 8 years of SAS programming working experience in the pharmaceutical industry.
• Good SAS programming skills and attention to details
• Demonstrated knowledge of regulatory guidelines, including electronic submission standards.
• Strong organizational, time management, communication, and project coordination and leadership skills.
• Must be able to work well under timeline pressure.
• Must be able to work on multiple tasks while coordinating others at the same time.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $88,300.00 - $220,900.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.