CrawlJobs Logo

Statistical Programmer II

parexel.com Logo

Parexel

Location Icon

Location:
Taiwan , Taipei

Category Icon
Category:
IT - Software Development

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

As a member of Parexel’s Statistical Programming group, you analyze, summarize, and graphically present clinical data to assess the safety and efficacy of the clinical trial. It requires attention to detail, a commitment to quality, and effective communication to ensure new treatments reach patients faster. You will work in different therapeutic areas assessing a variety of data entries and endpoints in an ever-changing environment. We provide a fertile environment for growth, with extensive training, mentoring, and technical knowledge sharing. You will work closely with the client and Parexel teams and collaborate to maximize the collective strength. Experience a supportive and motivating work environment where our teams offer an inherent breadth of knowledge within a diverse and inclusive workplace.

Job Responsibility:

  • Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation
  • Deliver best value and high quality service
  • Check own work in an ongoing way to ensure first-time quality
  • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings
  • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation
  • Maintain and expand local and international regulatory knowledge within the clinical industry
  • Develop knowledge of SAS and processes/procedures within other Parexel functional areas
  • Provide relevant training and mentorship to staff and project teams as appropriate
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulator compliance
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required
  • Proactively participate in process/quality improvement initiatives
  • Understand regulatory requirements concerning industry technical standards (e.g. CDISC, 21 CFR Part 11, and electronic submissions)

Requirements:

  • Excellent analytical skills
  • Proficiency in SAS
  • Knowledge and understanding of the programming and reporting process
  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
  • Ability to learn new systems and function in an evolving technical environment
  • Ability to manage competing priorities and flexibility to change
  • Attention to detail
  • Ability to successfully work as part of a global team
  • Work effectively in a quality-focused environment
  • Effective time management in order to meet daily metrics or team objectives
  • Show commitment to and perform consistently high quality work
  • Business/operational skills that include customer focus, commitment to quality management, and problem solving
  • Competent in written and oral English
  • Good communication skills
  • Educated to degree level in a relevant discipline and/or equivalent work experience
What we offer:
  • Flexible work arrangements
  • 'Bravo' Recognition Program

Additional Information:

Job Posted:
May 17, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Parexel - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Statistical Programmer II

Statistical Programmer II / SAS Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
South Africa , Remote
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Proficiency in SAS (Base, Macro, and Graph)
  • Sound knowledge of CDISC standards (ADaM, SDTM)
  • Proven clinical / statistical programming experience within pharmaceutical clinical development (CRO/Pharma) - Minimum 3years experience is essential
  • Strong analytical and communication skills
Job Responsibility
Job Responsibility
  • Develop and validate SAS programs for datasets, tables, listings, and figures
  • Collaborate with global teams to support clinical trial analysis
  • Ensure compliance with CDISC standards and regulatory requirements
  • 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
  • Contribute to life-changing research in a flexible, remote-friendly environment
What we offer
What we offer
  • Career growth and mentorship
  • Fully remote work options
  • A culture of integrity, respect, and innovation
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

Statistical Programmer II

As a member of Parexel's Statistical Programming group, you analyze, summarize, ...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent analytical skills
  • Proficiency in SAS
  • Knowledge and understanding of the programming and reporting process
  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
  • Ability to learn new systems and function in an evolving technical environment
  • Ability to manage competing priorities and flexibility to change
  • Attention to detail
  • Ability to successfully work as part of a global team
  • Work effectively in a quality-focused environment
  • Effective time management in order to meet daily metrics or team objectives
Job Responsibility
Job Responsibility
  • Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation
  • Deliver best value and high quality service
  • Check own work in an ongoing way to ensure first-time quality
  • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings
  • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation
  • Maintain and expand local and international regulatory knowledge within the clinical industry
  • Develop knowledge of SAS and processes/procedures within other Parexel functional areas
  • Provide relevant training and mentorship to staff and project teams as appropriate
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulator compliance
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required
What we offer
What we offer
  • Patient-led in everything we do
  • Supportive and inclusive environment
  • Opportunities for career growth
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Statistical Programmer II

As a member of Parexel's Statistical Programming group, you analyze, summarize, ...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Excellent analytical skills
  • Proficiency in SAS
  • Knowledge and understanding of the programming and reporting process
  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
  • Ability to learn new systems and function in an evolving technical environment
  • Ability to manage competing priorities and flexibility to change
  • Attention to detail
  • Ability to successfully work as part of a global team
  • Work effectively in a quality-focused environment
  • Effective time management in order to meet daily metrics or team objectives
Job Responsibility
Job Responsibility
  • Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation
  • Deliver best value and high quality service
  • Check own work in an ongoing way to ensure first-time quality
  • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings
  • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation
  • Maintain and expand local and international regulatory knowledge within the clinical industry
  • Develop knowledge of SAS and processes/procedures within other Parexel functional areas
  • Provide relevant training and mentorship to staff and project teams as appropriate
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulator compliance
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required
What we offer
What we offer
  • Flexible work arrangements
  • "Bravo" Recognition Program
  • Training programs
  • Mentoring
  • Knowledge sharing
  • Opportunities for career growth
  • Fulltime
Read More
Arrow Right

Statistical Programmer II

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
Taiwan , Taipei
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Educated to degree level in a relevant discipline and/or equivalent work experience
  • Competent in written and oral English
  • Good communication skills
  • Excellent analytical skills
  • Proficiency in SAS
  • Knowledge and understanding of the programming and reporting process
  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
  • Ability to learn new systems and function in an evolving technical environment
  • Ability to manage competing priorities and flexibility to change
  • Attention to detail
Job Responsibility
Job Responsibility
  • Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation
  • Deliver best value and high quality service
  • Check own work in an ongoing way to ensure first-time quality
  • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings
  • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation
  • Maintain and expand local and international regulatory knowledge within the clinical industry
  • Develop knowledge of SAS and processes/procedures within other Parexel functional areas
  • Provide relevant training and mentorship to staff and project teams as appropriate
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulator compliance
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required
What we offer
What we offer
  • Fertile environment for growth, with extensive training, mentoring, and technical knowledge sharing
  • Supportive and motivating work environment
  • Diverse and inclusive workplace
  • Opportunities for career growth
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Statistical Programmer II - FSP

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
India , Hyderabad
Salary
Salary:
Not provided
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Educated to degree level in a relevant discipline and/or equivalent work experience
  • Competent in written and oral English
  • Good communication skills
  • Excellent analytical skills
  • Proficiency in SAS
  • Knowledge and understanding of the programming and reporting process
  • Knowledge of SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11
  • Ability to learn new systems and function in an evolving technical environment
  • Ability to manage competing priorities and flexibility to change
  • Attention to detail
Job Responsibility
Job Responsibility
  • Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation
  • Deliver best value and high quality service
  • Check own work in an ongoing way to ensure first-time quality
  • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings
  • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation
  • Maintain and expand local and international regulatory knowledge within the clinical industry
  • Develop knowledge of SAS and processes/procedures within other Parexel functional areas
  • Provide relevant training and mentorship to staff and project teams as appropriate
  • Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulatory compliance
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required
What we offer
What we offer
  • Extensive training, mentoring, and technical knowledge sharing
  • Supportive and motivating work environment
  • Diverse and inclusive workplace
  • Opportunities for career growth
  • Flexible work arrangements
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
Read More
Arrow Right

Principal Statistical Programmer

As a member of Parexel’s Statistical Programming group, you analyze, summarize, ...
Location
Location
United States , Newton, Massachusetts
Salary
Salary:
159896.21 - 207400.00 USD / Year
parexel.com Logo
Parexel
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's in Statistics, Mathematics, Pharmaceutical Science, Data Analytics or related field. Employer will accept post-secondary academic coursework and/or relevant work experience which is evaluated as equivalent to a U.S. Bachelor’s degree in accordance with 8 CFR § 214.2(h)(4)(iii)(D)
  • 7 years of progressive experience in statistical programming
  • 7 years of experience with: Programming and reporting process
  • FDA 21 CFR Part 11 regulations
  • Regulatory requirements (ICH-GCP, CDISC, and electronic submissions)
  • Analyzing data from Phase I, II, and III clinical trials
  • SAS/BASE, SAS/STAT, SAS/SQL, SAS/MACRO, SAS Data Step, Proc Step, and Functions
  • Generating reports, tables, and listings for statisticians
  • Building structured, CDISC, SDTM, or ADaM databases for clinical studies
  • Leading teams in a statistical programming environment
Job Responsibility
Job Responsibility
  • Provide technical support and expert advice to internal and external sponsors on statistical programming projects to support clinical trial activities
  • Work independently to support various programming activities related to analysis and reporting of clinical study data
  • Fill the Statistical Programming Lead role on projects and liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas
  • Monitor quality, timelines, resource allocation, and productivity in relation to budget
  • Project management for statistical programming
  • Advise and negotiate statistical programming timelines
What we offer
What we offer
  • Employee Referral Program
  • Flexible work arrangements
  • Opportunities for career growth
  • Supportive and inclusive environment
  • Diverse therapeutic areas and project exposure
  • Advanced Technology
  • Fulltime
Read More
Arrow Right

Biostatistician II

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
  • Bachelor’s degree in Statistics or a related field
  • Experience in a biostatistics role in the pharmaceutical, clinical research, or healthcare industry is preferred
  • Proficiency in statistical concepts, study design, sample size calculations, and patient randomization
  • Familiarity with statistical analysis plans and the design of statistical tables, figures, and data listings for clinical reports
  • Strong data analysis skills, including data manipulation, retrieval, and interpretation
  • Proficiency in relevant computer languages and statistical software packages
  • Ability to write and implement programs to select, retrieve, manipulate, edit, and analyze data
  • Competency in assisting with statistical analyses and result interpretation
  • Effective communication and collaboration skills to work with cross-functional teams, including data management personnel, statistical programmers, and clinical research colleagues.
Job Responsibility
Job Responsibility
  • Assist senior biostatisticians in clinical study support, including study design, sample size calculations, patient randomization, data analysis, and results reporting
  • Support the statistical aspects of case report form design
  • Help in writing statistical analysis plans, defining derived data, and designing statistical tables and figures for clinical summary reports
  • Write data quality control specifications, utilize relevant computer languages and software
  • Develop and execute data manipulation and analysis programs
  • Assist in conducting statistical analyses and interpreting results
  • Prepare statistical summary reports and contribute to the statistical methods sections of integrated study reports
  • Review and document analysis and programming work for audit trail purposes
  • Contribute to project document standards and maintain project-specific biostatistics files
  • Collaborate effectively with ICON project team members, including data management, statistical programming, and clinical research personnel
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