Senior Standards Engineer

IQVIA; Durham (NC); Vor Ort; USD 98.000 - 273.000; Vollzeit

Zusammenfassung

IQVIA in Durham, NC is seeking a Senior Standards Engineer to ensure accuracy of statistical programming across clinical projects. The role emphasizes SAS programming and CDISC ADaM/SDTM standards.

You will develop and validate complex datasets, guide methodologies, mentor junior programmers, and drive improvements in workflows to ensure high-quality deliverables.

This position offers collaboration with cross-functional teams, and oversight of programming standards in a fast-paced environment.

Qualifikationen

• Bachelor's degree in statistics, CS or related field required.
• Master's degree preferred; ability to lead and manage others.
• Strong confidentiality and judgment in handling data.
• Ability to work under tight deadlines and manage time/resources.

Aufgaben

• Develops and validates complex datasets and outputs using SAS, aligning with CDISC ADaM/SDTM.
• Collaborates with cross-functional teams to optimize programming processes.
• Provides technical guidance on statistical methodologies for trials.
• Mentors junior programmers and fosters their growth.
• Drives continuous improvement of workflows and departmental standards.
• Ensures high-quality deliverables by adhering to best practices and protocols.
• Leads initiatives to enhance tools and techniques in programming.
• Partners with leadership to align objectives with organizational goals.

Kenntnisse

SAS programming

CDISC standards

ADaM/SDTM

Statistical programming leadership

Mentoring

Data validation

Process optimization

Statistical methods

Confidentiality

Project management

Ausbildung

Bachelor's Degree in Statistics, Computer Science or related field

Master's Degree in Statistics or Computer Science

Tools

SAS

CDISC

ADaM

SDTM

Jobbeschreibung

Job Overview

The Senior Standards Engineer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in SAS programming and familiarity with CDISC standards, particularly ADaM and SDTM models.

Key responsibilities include developing and validating complex data sets and outputs, collaborating with cross-functional teams to optimize processes, and providing technical guidance on statistical methodologies and programming best practices. The role also involves mentoring junior programmers and contributing to the continuous improvement of programming workflows and standards, supporting the overall quality deliverables of the statistical programming department.

Essential Functions

• Develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards such as ADaM and SDTM models.
• Collaborates with cross-functional teams to optimize statistical programming processes and enhance overall efficiency and accuracy.
• Provides technical guidance and expertise on statistical methodologies to support clinical trial projects and departments.
• Mentors and guides junior programmers, fostering their growth and development.
• Contributes to the continuous improvement of programming workflows and departmental standards.
• Ensures high-quality deliverables from the statistical programming department by adhering to best practices and established protocols.
• Leads initiatives to enhance programming tools and techniques, driving innovation in statistical programming.
• Partners with leadership to align programming objectives with larger organizational goals.

Qualifications

• Bachelor's Degree Statistics, Computer Science or related field
• Req Master's Degree Statistics or Computer Science Pref Ability to lead/manage others.
• Capably leads and manages programming teams, ensuring adherence to standards and mentoring junior programmers.
• Demonstrated ability to maintain confidential information.
• Maintains strict confidentiality of sensitive project data and internal communications
• Demonstrates excellent judgment and decision-making skills.
• Exercises sound judgment and decision-making in selecting statistical methods and programming techniques.
• Ability to work within tight timeframes and meet strict deadlines. Effectively manages time and resources to deliver high-quality programming outputs within tight deadlines.
• Demonstrated project management skills. Executes projects efficiently, demonstrating strong project management skills to coordinate tasks and resources effectively.
• Possesses strong technical aptitude. Demonstrates robust technical aptitude with a deep understanding of SAS programming and CDISC standards.
• Analyze and interpret financial data. Analyses and interprets financial data accurately to make informed decisions in statistical programming.
• Demonstrated analytical skills. Utilizes strong analytical skills to assess statistical programming requirements and ensure data integrity.
• Demonstrated problem solving skills. Applies effective problem-solving skills to overcome programming challenges and optimize workflows.
• Excellent interpretation of complex statistical data. Interprets complex statistical data with proficiency, ensuring accurate construction and validation of clinical datasets.
• Demonstrated written communication skills. Exhibits strong written communication skills to document programming methodologies and procedures clearly.
• Strong verbal communication and listening skills. Communicates effectively with cross-functional teams to facilitate collaboration and improve statistical programming processes.
• Instills commitment to organizational goals. Inspires and motivates programming teams to align their work with organizational goals and quality standards.

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.

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. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $98,200.00 - $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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments.

Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.