ADaM Standards Engineer, FSP

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

Job summary

An established industry player is seeking an ADaM Standards Engineer to join a dedicated team supporting a leading Pharma company's standards initiatives. This role focuses on developing and maintaining ADaM standards, ensuring compliance with CDISC and regulatory requirements. The ideal candidate will possess a strong background in statistical programming with over 8 years of experience, alongside expertise in SDTM and ADaM standards. Join a forward-thinking company committed to advancing medical treatments and improving patient outcomes through innovative research. This is a unique opportunity to make a significant impact in the life sciences sector while working in a collaborative and dynamic environment.

Qualifications

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

Responsibilities

• Develop and maintain ADaM standards for clinical trials.
• Review SDTM standards and ensure compliance.
• Support data standards development and submission.

Skills

CDISC Standards Implementation

Problem Solving

Oral & Written Communication

Attention to Detail

Self-Motivation

Multi-tasking

Team Working Skills

Education

Bachelor's Degree in Computer Science

Bachelor's Degree in Math

Bachelor's Degree in Statistics

Bachelor's Degree in Biology

Bachelor's Degree in Pharmacology

Tools

Statistical Programming

ADaM Standards

SDTM Standards

Job description

ADaM Standards Engineer, FSP

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:

• 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.