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Parexel

End-to-end clinical trials and regulatory consulting

Senior Statistical Programmer

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeTaipei City, TaiwanNo salary listedIn-person

About the Job

Requirements

  • Proficiency in SAS.
  • Extensive knowledge and understanding of the programming and reporting process.
  • Knowledge of SOPs/Guidelines, ICH-GCP, and applicable local and international regulations, including 21 CFR Part 11.
  • Ability to learn new systems and function in an evolving technical environment.
  • Strong project management skills.
  • Strong organizational skills and ability to manage competing priorities and adapt to change.
  • Attention to detail.
  • Ability to lead a global team.
  • Ability to work effectively in a quality-focused environment.
  • Effective time management to meet daily metrics or team objectives.
  • Commitment to consistently high-quality work.
  • Business and operational skills, including customer focus, quality management, and problem solving.
  • Commitment to refining quality processes.
  • Good presentation skills.
  • Business awareness and business development skills, including financial awareness.
  • Competence in written and oral English.
  • Degree-level education in a relevant discipline or equivalent work experience.

Responsibilities

  • Fill the Statistical Programming Lead role on projects when required.
  • Provide input into and negotiate statistical programming timelines, ensure adherence to timelines, coordinate and lead statistical programming teams to complete studies within timelines and budget, monitor project resourcing and budgets, and identify changes in scope.
  • Coordinate project start-up activities and create global programs, tracking spreadsheets, and other required documentation.
  • Review statistical analysis plans, mock shells, and database set-up specifications.
  • Interact with sponsors and internal stakeholders regarding statistical programming issues.
  • Assist project teams in resolving problems encountered in daily work.
  • Deliver high-value, high-quality statistical programming services and check own work on an ongoing basis to ensure first-time quality.
  • Use efficient programming techniques to produce and quality-check derived datasets such as SDTM and ADaM, tables, figures, and data listings.
  • Produce and quality-check dataset specifications, process-supporting documents, and submission documentation.
  • Ensure quality control of process and technical activities related to derived datasets, tables, data listings, and figure programming in accordance with corporate quality standards, SOPs/Guidelines, ICH-GCP, and applicable international regulatory requirements.
  • Maintain and expand local and international regulatory knowledge within the clinical industry.
  • Develop knowledge of SAS and processes and procedures within other Parexel functional areas.
  • Provide relevant training and mentorship to staff and project teams.
  • Maintain study-supporting documentation in accordance with SOPs/Guidelines to ensure traceability and regulatory compliance.
  • Ensure compliance with SOPs/Guidelines, ICH-GCP, and applicable local and international regulations, and participate in internal and external audits and regulatory inspections as required.
  • Participate in and/or lead process and quality improvement initiatives.
  • Provide consultancy to internal and external sponsors on statistical programming tasks.
  • Represent Parexel at sponsor marketing and technical meetings.
  • Understand regulatory requirements concerning industry technical standards, including CDISC, 21 CFR Part 11, and electronic submissions.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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