CrawlJobs Logo
iconplc Logo iconplc · IT - Software Development

Senior Clinical Data Science Programmer

Mexico, Mexico City · Job Posted March 21, 2026
Apply Position
Job Link Share

Job Description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming expertise.

Job Responsibility

  • Developing, validating, and maintaining programming solutions for data analysis and reporting in clinical trials
  • Collaborating with clinical data scientists and biostatisticians to ensure the integration of programming solutions into the overall data management process
  • Overseeing the generation of statistical datasets, tables, listings, and figures to support regulatory submissions and study reports
  • Providing guidance on programming best practices, coding standards, and data quality control measures
  • Staying updated on advancements in programming languages and data management tools to enhance operational efficiencies

Requirements

  • Advanced degree in a relevant field such as computer science, statistics, or life sciences
  • Extensive experience in programming for clinical trials, with proficiency in languages such as SAS, R, or Python
  • Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment
  • Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results
  • Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes

What we offer

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
iconplc - All Job Offers

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Suggested Tags: Frontend Developer Secretary Talent Manager Salesforce Administrator Data Analyst
Similar Jobs for

Senior Clinical Data Science Programmer

8 matching positions

Senior Lead Clinical Data Science Programmer

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in Data Science, Statistics, Computer Science, or a related field
  • advanced certifications in data programming or clinical data science are advantageous
  • Extensive experience in clinical data programming, with a strong background in statistical analysis, data management, and programming languages such as SAS, R, or Python
  • Proven ability to lead and manage programming teams, and develop data science solutions that support clinical research objectives
  • Strong analytical skills, with experience in designing and implementing complex data analysis and visualization techniques
  • Excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams and present data insights to stakeholders.
Job Responsibility
Job Responsibility
  • Use technical, industrial, and interpersonal skills to ensure assigned project and business initiative programming deliverables are met on a team or portfolio level and within service and quality expectations
  • Provide technical oversight as required and mentoring and developing other members of the Clinical Data Science Programming team
  • Represent CDS programming team on cross-project or cross-department projects
  • Actively participate in internal meetings and provides constructive feedback to peers, team leads and managers, and functional management
  • Organise, create, and oversees the administration of training and mentoring for junior levels
  • Support knowledge sharing within the peer group through presentations and preparation of training materials
  • Development of materials for the bid defence process and client demonstrations
  • May act as a subject matter expert (SME) within a specific area of the team, and lead teams of other SMEs
  • Considered an expert in all areas of clinical data science programming for clinical trials.
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Read More
Arrow Right

Senior Clinical Python Programmer

Sr Clinical Programmer (Phyton) - Mexico - Remote. ICON plc is a world-leading h...
Location
Location
Mexico , Mexico City
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Degree in Data Science, Statistics, Computer Science, or a related field
  • advanced certifications in data programming or clinical data science are advantageous
  • extensive experience in clinical data programming, with a strong background in statistical analysis, data management, and programming languages such as SAS, R, or Python
  • proven ability to lead and manage programming teams, and develop data science solutions that support clinical research objectives
  • strong analytical skills, with experience in designing and implementing complex data analysis and visualization techniques
  • excellent communication and leadership skills, with the ability to collaborate effectively with cross-functional teams and present data insights to stakeholders
  • willingness to travel as required (approximately 10%)
Job Responsibility
Job Responsibility
  • Leading the design, development, and validation of data science programming solutions to support clinical trials, including data integration, statistical analysis, and reporting
  • managing and mentoring a team of clinical data programmers, providing guidance and ensuring adherence to programming standards and best practices
  • collaborating with clinical research teams and stakeholders to define data requirements, develop programming specifications, and implement data science methodologies
  • overseeing data quality assurance processes, including data validation and verification, to ensure the accuracy and completeness of clinical trial data
  • utilizing advanced statistical techniques and data visualization tools to analyze complex data sets and generate actionable insights for clinical research
  • staying current with industry trends and advancements in data science and clinical research, and recommending innovative solutions to enhance data analysis and reporting
What we offer
What we offer
  • Various annual leave entitlements
  • a range of health insurance offerings to suit you and your family’s needs
  • competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • life assurance
  • flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
  • Fulltime
Read More
Arrow Right

Senior Clinical Database Programmer

The Senior Clinical Database Programmer is responsible for the programming of hi...
Location
Location
India , Remote
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Life Science, Computer Science or equivalent
  • Minimum of 5 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
  • Technical skills and experience using relational databases (e.g. Oracle InForm, Rave EDC System, Oracle DMW, MS SQL Server or MS Access)
  • Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills
  • Rave Custom Function Programming skills are mandatory
  • Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills
  • Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
  • Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)
  • Understanding regulatory requirements and relevant data standards
  • CDISC knowledge and experience are preferable
Job Responsibility
Job Responsibility
  • Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans
  • Complies with applicable SOPs and work practices
  • Serves as subject matter expert in one or more technologies
  • Leads and contributes to cross-functional technical initiatives in collaboration with clients Digital and other teams
  • Supports knowledge development of data capture tools and methods that support the accuracy and integrity of study data
Read More
Arrow Right

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
Poland , Warsaw
Salary
Salary:
200000.00 - 278000.00 PLN / Year
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
  • Proficiency in SAS
  • Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
  • Demonstrated proficiency in analytical programming
  • Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
  • Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
  • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
  • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
  • Have good understanding of regulatory, industry, and technology standards and requirements
  • Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs
Job Responsibility
Job Responsibility
  • Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
  • Perform programming validation to ensure quality of analysis datasets and programming outputs
  • Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
  • Support the electronic submission preparation and review
  • Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
  • Assesses impact on programming activities
  • Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
  • Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
  • Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
  • Independently leads and / or performs programming assignments with minimal supervision
What we offer
What we offer
  • Fully flexible work arrangement
  • Opportunity to use Warsaw office if desired
  • Annual performance-based bonus plan (for eligible roles)
  • Annual salary review
  • Total rewards incentives
  • Extensive training, mentoring, and technical knowledge sharing
  • Opportunities for career growth
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced technology
  • Fulltime
Read More
Arrow Right

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
Poland; Serbia
Salary
Salary:
200000.00 - 278000.00 PLN / Year
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
  • Proficiency in SAS
  • Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
  • Demonstrated proficiency in analytical programming
  • Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
  • Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
  • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
  • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
  • Have good understanding of regulatory, industry, and technology standards and requirements
  • Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs
Job Responsibility
Job Responsibility
  • Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
  • Perform programming validation to ensure quality of analysis datasets and programming outputs
  • Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
  • Support the electronic submission preparation and review
  • Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
  • Assesses impact on programming activities
  • Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
  • Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
  • Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
  • Independently leads and / or performs programming assignments with minimal supervision
What we offer
What we offer
  • Flexible work arrangements
  • Opportunities for career growth
  • Supportive and inclusive environment
  • Annual performance-based bonus plan
  • Annual salary review
  • Total rewards incentives
  • Fulltime
Read More
Arrow Right

Senior Statistical Programmer

ICON plc is a world-leading healthcare intelligence and clinical research organi...
Location
Location
United Kingdom , Reading
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field
  • Significant experience in statistical programming within the clinical research or pharmaceutical industry
  • Strong proficiency in SAS programming and a solid understanding of statistical concepts and methodologies
  • Excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously
  • Strong communication and interpersonal skills, with the ability to work collaboratively within a multidisciplinary team
Job Responsibility
Job Responsibility
  • Designing, developing, and validating SAS programs for statistical analysis and reporting of clinical trial data
  • Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods
  • Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines
  • Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs
  • Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right

Senior Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
Serbia; Poland
Salary
Salary:
200000.00 - 278000.00 PLN / Year
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required
  • Proficiency in SAS
  • Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development
  • Demonstrated proficiency in analytical programming
  • Have in-depth understanding of clinical data structure (e.g., CDISC standards) and relational databases
  • Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21
  • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM
  • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission
  • Have good understanding of regulatory, industry, and technology standards and requirements
  • Have good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs
Job Responsibility
Job Responsibility
  • Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures
  • Perform programming validation to ensure quality of analysis datasets and programming outputs
  • Provides programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis
  • Support the electronic submission preparation and review
  • Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
  • Assesses impact on programming activities
  • Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers
  • Provides leadership for ensuring quality of deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices
  • Identifies opportunities for increased efficiency and consistency within team and our interactions with strategic vendors
  • Independently leads and / or performs programming assignments with minimal supervision
What we offer
What we offer
  • Fully flexible work arrangement - you can be fully home based
  • Annual performance-based bonus plan
  • Annual salary review
  • Total rewards incentives
  • Extensive training, mentoring, and technical knowledge sharing
  • Opportunities for career growth
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Senior Statistical Programmer II

Statistical Programmer II, Canada, Remote. ICON plc is a world-leading healthcar...
Location
Location
Canada , Montreal
Salary
Salary:
Not provided
iconplc.com Logo
iconplc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field
  • Significant experience in statistical programming within the clinical research or pharmaceutical industry
  • Strong proficiency in SAS programming and a solid understanding of statistical concepts and methodologies
  • Excellent analytical skills, attention to detail, and the ability to manage multiple projects simultaneously
  • Strong communication and interpersonal skills, with the ability to work collaboratively within a multidisciplinary team
Job Responsibility
Job Responsibility
  • Designing, developing, and validating SAS programs/R-Shiny applications for statistical analysis and reporting of clinical trial data
  • Working closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods
  • Performing quality control checks and reviewing statistical outputs to ensure compliance with project specifications and regulatory guidelines
  • Assisting in the preparation of statistical reports, presentations, and regulatory submissions to support clinical development programs
  • Mentoring junior programmers and contributing to team development by sharing best practices and technical knowledge
What we offer
What we offer
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others
Read More
Arrow Right