Principal Statistical Programmer, Standards

IQVIA; Durham (NC); Remote; USD 88,000 - 274,000; Full time

Job summary

A leading healthcare and clinical research firm is seeking a Principal Statistical Programmer to support standards initiatives. The ideal candidate will have 8+ years' experience and expert knowledge of SDTM and ADaM standards. This remote position allows for flexible work across the United States or Canada.

Qualifications

• 8+ years of experience as a Statistical Programmer.
• Expert knowledge of SDTM and ADaM data standards.
• Prefer therapeutic experience in Oncology, Virology, or Inflammation.

Responsibilities

• Support activities for Clinical Data Standards development.
• Lead study-related programming activities.
• Review and provide feedback on e-submission packages.

Skills

Problem solving

Oral communication

Written communication

Attention to detail

Multi-tasking

Team working

Education

Bachelor's degree in a relevant field

Job description

Principal Statistical Programmer, Standards

Location: home-based anywhere in the United States or Canada

Position Summary:

IQVIA is hiring to expand a sponsor-dedicated team, working fully within the environment of a prominent Pharma company, supporting their long-term standards initiatives. The ADaM Standards Engineer will act as ADaM Standards SME in development of standards management strategy and ongoing development and maintenance of standards across the client’s portfolio. This role does not involve actual study work but requires a high degree of self-motivation/direction and attention to detail, as well as exceptional problem solving, oral & written communication, multi-tasking, and team working skills.Previous experience with implementing CDISC standards that supports strategies and processes for clinical trials is required.

Responsibilities:

• Support activities related to Sponsor specific Clinical Data Standards development and maintenance such as standardizing SDTM and ADaM Specifications and TFLs across therapeutic areas and within specific projects
• Support client specific SDTM and ADaM mapping tools
• Review e-submission packages and provide feedback.
• Leading study-related programming activities for a molecule (writing specification for ADaM, ADaM/TLF programming & validation for both Safety & efficacy), primarily involving legacy data.
• Develop, update, and maintain ADaM standards.
• Review SDTM standards for updates and impacts on current ADaM CORE standards.
• Participate in study specific ADaM submission package reviews across multiple authorities.
• Provides technical and/or operational support in the delivery and application of industry clinical data standards within the statistical programming data flow (i.e., SDTM, ADaM, DEFINE) for clinical studies, drug programs, and/or in support of drug application submissions.
• Identifies data inconsistencies with respect to data standards compliance and proposes solutions that support data review/efficiencies including ensuring robust master dataset specifications and correct interpretation of protocol, analysis, and CDISC compliance requirements.
• Ensures study level ADaM datasets are in compliance with CDISC and regulatory submission requirements, reviews study submission data packages to ensure quality and integrity.
• Works closely with study leads and Data Management on development of data standards to support data collection requirements; including but not limited to specification of Data transfer agreements (DTAs) in alignment with downstream SDTM and other dataset formats, CRF Standard data collection elements, and external data oversight/strategies to ensure downstream compliance for submission.
• Support in developing, managing, and maintaining libraries of CDISC-related metadata, terminology, and related standards. Provides governance oversight to ensure consistency in metadata use and development.
• Actively monitors for new regulatory requirements related to data standards and/or data submissions; Communicates and provides impact assessment / consultancy to Data Sciences or specific project teams.

Qualifications:

• Bachelor's degree in computer science, math, statistics, biology, pharmacology, or related.
• 8+ years’ experience as a Statistical Programmer with recent experience working on a Global Standards team or have created Global Standards within a Sponsor or CRO environment
• Expert knowledge of SDTM and ADaM data standards and FDA/PMDA/EMA submission requirements required
• Therapeutic experience in Oncology, Virology, and/or Inflammation is preferred.

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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 athttps://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

The potential base pay range for this role, when annualized, is $88,300.00 - $273,200.00. 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.