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Parexel

End-to-end clinical trials and regulatory consulting

Statistical Programmer 1

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeShanghai, ChinaNo salary listedIn-person

About the Job

Requirements

  • Proficiency in SAS.
  • Knowledge and understanding of the programming and reporting process.
  • Knowledge of standard operating procedures and guidelines, ICH-GCP, and applicable local and international regulations, including 21 CFR Part 11.
  • Competence in written and oral English.
  • A degree in a relevant discipline or equivalent work experience.
  • Ability to learn new systems and function in an evolving technical environment.
  • Ability to manage competing priorities and adapt to change.
  • Ability to work effectively as part of a global team and in a quality-focused environment.
  • Effective time management to meet daily metrics or team objectives.
  • Business and operational skills including customer focus, commitment to quality management, and problem solving.

Responsibilities

  • Assist in coordinating project start-up activities, creating global programs and tracking spreadsheets, and preparing other required documentation.
  • Produce derived datasets, tables, figures, and data listings of any complexity using efficient programming techniques, and quality-check low- to medium-complexity derived outputs.
  • Assist with producing and quality-checking derived dataset specifications, process-supporting documents, and submission documentation.
  • Maintain and expand local and international regulatory knowledge within the clinical industry.
  • Develop knowledge of SAS and processes and procedures in other Parexel functional areas.
  • Provide relevant training and mentorship to staff and project teams as appropriate.
  • Maintain study supporting documentation in accordance with standard operating procedures and guidelines to ensure traceability and regulatory compliance.
  • Ensure compliance with standard operating procedures and guidelines, ICH-GCP, and applicable local and international regulations; participate in internal and external audits and regulatory inspections as required.
  • Participate proactively in process and quality improvement initiatives.
  • Understand regulatory requirements for industry technical standards, including CDISC, 21 CFR Part 11, and electronic submissions.
  • Check own work on an ongoing basis to ensure first-time quality.
  • Deliver high-value, high-quality service and consistently perform quality work.

Desired Qualifications

  • Excellent analytical skills.
  • Good communication skills.
  • Attention to detail.

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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