Home
/
Comprehensive
/
Principal Statistical Programmer
Principal Statistical Programmer-February 2024
Durham
Feb 10, 2026
About Principal Statistical Programmer

  Location: Homebased anywhere in the US

  Purpose:

  Experienced R programmers needed to provide technical expertise to develop process methodology for department to meet internal and external clients’ needs. 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

  Home Based

  Min 4+ years of CRO/Pharma Industry

  Therapeutic Areas: Oncology // Immunology // IDV // EDCP

  Key Skills:

  Must have expertise of R programming as well as 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.

  Minimum of 4+ 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

  Ability to delegate work to other members of the SP team [SPM]

  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 co-ordinate 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 reputable university preferably in science/ mathematics related fieldsIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

  We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

  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. https://jobs.iqvia.com/covid-19-vaccine-status

  The potential base pay range for this role, when annualized, is $119,400.00 - $203,100.00. 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.

  IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

  To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

  EEO Minorities/Females/Protected Veterans/Disabled

Comments
Welcome to zdrecruit comments! Please keep conversations courteous and on-topic. To fosterproductive and respectful conversations, you may see comments from our Community Managers.
Sign up to post
Sort by
Show More Comments
SIMILAR JOBS
Shift Supervisor Trainee
Bring your heart to CVS Health. Every one of us at CVS Health shares a single, clear purpose: Bringing our heart to every moment of your health. This purpose guides our commitment to deliver enhanced
RN Vascular FT
PURPOSE AND SCOPE: Supports the Organization mission, vision, core values and customer service philosophy. Adheres to the Organization Compliance Program, including following all regulatory and Organi
Equipment Operator - 29$ And Up- APPLY NOW!
IMMEDIATE HIRING FOR EQUIPMENT OPERATOR/CONSTRUCTION PAY RATE -29$/HOUR APPLY NOW! Description: The primary function of this position will be operating a 12-ton lull and moving materials that other su
Charge Registered Nurse
PURPOSE AND SCOPE: Works with the Facility Manager, facility staff and physician to coordinate the facility operations and patient procedures to ensure provision of quality patient care on a daily bas
Medical Information Specialist with German, Czech Republic
Job Description Medical Information Specialist with German, Czech Republic At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleag
Director - Value & Access Consulting - Evidera
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customer
UX Designer, Project Tapestry
UX Designer, Project Tapestry User Experience Design Mountain View, CA X is Alphabet’s moonshot factory. We are a diverse group of inventors and entrepreneurs who build and launch technologies that ai
Truck Driver on-the-job CDL Training
Roehl Transport Paid CDL Training Truck Driver JobTime for a Change?Make more of yourself and for yourself. Roehl Transport will pay you to get your CDL earn a great a living as a professional truck d
Project Engineer Payload Integration
Highlights Working For GA-ASI: This position is eligible for the Individual Compensation Program (ICP) bonus. This position is eligible for a hybrid work environment pending project needs. Outstanding
Receiving Clerk
Job Number 24087001 Job Category Procurement, Purchasing, and Quality Assurance Location Renaissance Sharm El Sheikh Golden View Beach Resort, Al Fanar Street, Sharm El Sheikh, Egypt, Egypt Schedule F
Copyright 2023-2026 - www.zdrecruit.com All Rights Reserved