×
Register Here to Apply for Jobs or Post Jobs. X

Principal Statistical Programmer - FSP and Remote

Remote / Online - Candidates ideally in
Durham, Durham County, North Carolina, 27703, USA
Listing for: IQVIA
Remote/Work from Home position
Listed on 2026-03-10
Job specializations:
  • IT/Tech
    Data Analyst, IT Consultant
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Location:

Homebased anywhere in the US

Join our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Job Details
  • Position: – Principal Statistical Programmer
  • Location: Home Based
  • Experience: Min 7+ years of CRO/Pharma Industry
  • Thematic Areas: Oncology // Immunology // IDV // EDCP
Key Skills
  • 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.
  • Minimum of 7+ years of experience in Statistical Programming in pharmaceutical or medical devices industry.
  • Good verbal and written communication skills.
  • Ability to work on multiple projects, plan, organize and prioritize activities.
Required Knowledge,

Skills and Abilities
  • Experience as technical team lead directly engaging clients and coordinating tasks within a programming team.
  • In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Knowledge of statistics, programming and/or clinical drug development process.
  • Advanced knowledge of R programming.
  • Base SAS, SAS/STAT, SAS Graph and SAS Macro Language.
  • Should have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.
  • Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.
  • Good organizational, interpersonal, leadership and communication skills.
  • Ability to independently manage multiple tasks and projects.
  • Ability to delegate work to other members of the SP team.
  • Excellent accuracy and attention to detail.
  • Exhibits routine and occasionally complex problem-solving skills.
  • Ability to lead teams and projects and capable of managing at a group level.
  • Recognizes when negotiating skills are needed and seeks assistance.
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Responsibilities
  • Perform, plan, coordinate and implement complex study programming, testing, and documentation of statistical programs for use in creating tables, figures, listings, and analysis datasets; also handle transfer files and perform quality control checks.
  • Interpret project level requirements and develop programming specifications for complex studies.
  • Provide advanced technical expertise in conjunction with internal and external clients, independently bringing project solutions to SP teams and the Statistical Programming department.
  • Fulfill project responsibilities as technical team lead for single complex studies or a 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…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary