Sr Cra - Sponsor Dedicated - Argentina Home Based

7257 Syneos Health Argentina S.A.; Quilmes; À distance; ARS 139 086 000 - 200 903 000; Plein temps

Avantages offerts par ce poste

Sponsor dedicated - 100% Home based

Résumé du poste

IQVIA is seeking a Senior Statistical Programmer for Pharmacometrics support. The role focuses on R and SAS programming, with CDISC ADaM/SDTM expertise, delivering validated datasets and outputs across clinical projects. Collaboration with cross-functional teams is essential, as is mentoring junior programmers.

The position is 100% home-based with a focus on LATAM regions. Strong English skills and leadership capabilities are required to ensure high-quality deliverables and adherence to

Qualifications

• Proficiency in R and SAS programming.
• CDISC standards proficiency (ADaM and SDTM).
• Bachelor’s degree in Statistics, Computer Science or related field.

Responsabilités

• Develops and validates complex datasets and outputs using SAS, ensuring CDISC ADaM/SDTM compliance.
• Collaborates with cross-functional teams to optimize statistical programming processes.
• Provides technical guidance on statistical methodologies and programming best practices.
• Mentors junior programmers and contributes to workflow improvements.

Connaissances

R programming

SAS programming

CDISC (ADaM/SDTM)

Leadership/mentoring

Statistical programming

Formation

Bachelor's Degree in Statistics/CS or related field

Outils

SAS

Description du poste

Senior Statistical Programmer in Pharmacometrics (PM) support (Clinical Trials)

Mexico City, Mexico
Santiago, Chile
Buenos Aires, Argentina
Lima, Peru
Quito, Ecuador
São Paulo, Brazil
Bogota, Colombia
Full time
R
Sponsor dedicated - 100% Home based role.
Job Overview
The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in R and 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.
• 2 + years working with efficacy analysis (Adam datasets & TLF's) and/or 4 + years on ADAM statistical programming on clinical trials.
• Hands-on proficiency in R programming language (mandatory).
• Proficiency in SAS programming language.
• Advanced English (both written and spoken - tested during the interview process).
• Native language is required - LATAM: Spanish or Portuguese.
• 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, sensitive project data and internal communications.
• Exercises sound judgment and decision-making in selecting statistical methods and programming techniques.
• Effectively manages time and resources to deliver high-quality programming outputs within tight deadlines.
• Executes projects efficiently, demonstrating strong project management skills to coordinate tasks and resources effectively.
• Demonstrates robust technical aptitude with a deep understanding of SAS programming and CDISC standards.
• Analyses and interprets financial data accurately to make informed decisions in statistical programming.
• Applies effective problem-solving skills to overcome programming challenges and optimize workflows.
• Exhibits strong written and verbal communication skills to document programming methodologies and procedures clearly to facilitate collaboration and improve statistical programming processes with cross-functional teams.
• Inspires and motivates programming teams to align their work with organizational goals and quality standards.

Important: submit your CV in English.
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 at 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.
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.
EEO Minorities/Females/Protected Veterans/Disabled

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office

Job Description
Join Us as a Clinical Trial Coordinator II - Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you'll have the opportunity to provide administrative and technical support to the Project Team. ...EEO Minorities/Females/Protected Veterans/Disabled

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