Clinical Data Programming Lead

ICON plc

Clinical Data Programming Lead at ICON, designing and analyzing clinical trials. Overseeing data programming activities and collaborating with cross-functional teams to ensure compliance and quality.

Posted 7/7/2026full-timeMexico City • 🇲🇽 MexicoSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical data programming, including proficiency in SAS, Python, and SQL, while ensuring compliance with CDISC standards and FDA/EMA regulations. Proven leadership in guiding programming teams and enhancing data quality through innovative solutions.

Highest-signal resume keywords

Clinical Data ProgrammingSAS ProgrammingPython ProgrammingSQL ProgrammingCDISC Standards

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ProgrammingSAS ProgrammingPython ProgrammingSQL ProgrammingData AnalysisRegulatory ComplianceProgramming Best PracticesData Quality AssuranceStatistical AnalysisTroubleshooting Support

Soft Skills

LeadershipCommunicationProblem-SolvingDecision-MakingCollaboration

Industry Keywords

Pharmaceutical IndustryBiotechnologyCRO IndustryFDA RegulationsEMA RegulationsICH-GCP Guidelines

Tech Stack

Tools & technologies

Google Cloud PlatformPythonSQL

About the role

Key responsibilities & impact

Lead and oversee the clinical data programming activities across multiple clinical trials, ensuring quality, timeliness, and compliance with regulatory requirements
Collaborate with cross-functional teams to develop programming strategies and standards for data collection, processing, and analysis
Provide technical expertise and guidance to programming team members, including programming best practices and troubleshooting support
Review and validate programming deliverables, ensuring accuracy, consistency, and adherence to predefined specifications
Contribute to the development and implementation of innovative programming solutions to enhance efficiency and data quality in clinical trials

Requirements

What you’ll need

Bachelor's degree or higher in Computer Science, Statistics, or a related field
Prior experience in clinical data programming within the pharmaceutical, biotechnology, or CRO industry
Proven leadership experience, with the ability to effectively lead and mentor a team of programming professionals
Expertise in programming languages commonly used in clinical research, such as SAS, Python, and/or SQL
Strong understanding of CDISC standards, FDA/EMA regulations, and ICH-GCP guidelines
Excellent communication, problem-solving, and decision-making skills, with a focus on driving results and fostering collaboration
Willingness to travel as required (approximately 15%)

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways