Principal Statistical Programmer

4 weeks ago


Baltimore, Maryland, United States 5PY US Quintiles, Inc. Full time
Job Title: Principal Statistical Programmer

Location: Home-based in the US

Purpose:

As a Principal Statistical Programmer, you will play a key role in planning and coordinating the development of integrated programming solutions for our clients. You will provide technical expertise and leadership to the department, ensuring that projects are completed on time and to the highest standards.

Job Details:

Position: Principal Statistical Programmer

Home Based: Yes

Min 4+ years of CRO/Pharma Industry: Yes

Therapeutic Areas: Oncology, Immunology, IDV, EDCP

Key Skills:

Must have expertise in R programming, SAS Base, and good knowledge of SAS graph and SAS Macros. Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician. Must have excellent knowledge of CDISC standards (SDTM and ADaM). Thorough understanding of relational database components and theory. Excellent application development skills. Strong understanding of clinical trial data and extremely hands-on in data manipulations, analysis, and reporting of analysis results. Good understanding of ICH E6, ICH E3, ICH E8, ICH E9, and clinical research processes.

Responsibilities:

Perform, plan, coordinate, and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files for internal and external clients and (iii) the programming quality control checks for the source data and report the data issues periodically. Ability to interpret project-level requirements and develop programming specifications, as appropriate, for complex studies. Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies. Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies. Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines. Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables. Use and promote the use of established standards, SOP, and best practices. Provide training and mentoring to SP team members and Statistical Programming department staff.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE:

Bachelor's degree from a reputable university preferably in science/mathematics-related fields. 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://www.iqvia.com/. We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.

The potential base pay range for this role, when annualized, is $117, $218. 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.



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