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Senior Statistical Programmer – R Programming

🕒 August 25

⏰ Full Time

🟠 Senior

🖥 Software Engineer

Where this job comes from

Posted on Parexel's careers page, not through a job board

First seen by Remote Rocketship August 25

Still open on Parexel's site. Checked 11 hours ago.

Logo of Parexel

Parexel

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Provide technical expertise for clinical trial conduct and support programming activities related to clinical study data analysis and reporting • Serve as an internal subject matter expert and provide technical support and expert advice • Fill the Statistical Programming Lead role on projects when needed • Liaise with sponsors, Biostatistics Leads, Data Management Leads, and other functional areas • Monitor quality, timelines, resource allocation, productivity, and budgets • Negotiate and maintain statistical programming timelines • Coordinate and lead statistical programming teams to complete studies within timelines and budget • Monitor project resourcing and budgets and identify scope changes • Coordinate project start-up activities and create global programs, tracking spreadsheets, and documentation • Review statistical analysis plans, mock-shells, and database set-up specifications • Produce and QC derived datasets, tables, figures, and data listings using efficient programming techniques • Produce and QC dataset specifications, process-supporting documents, and submission documentation • Ensure QC and compliance with corporate quality standards, SOPs/Guidelines, ICH-GCP, and international regulatory requirements • Provide training, mentorship, and consultancy to staff, project teams, and sponsors • Maintain study documentation for traceability and regulatory compliance • Participate in audits, regulatory inspections, and process/quality improvement initiatives • Represent Parexel at sponsor marketing and technical meetings • Understand and apply standards including CDISC, 21 CFR Part 11, and electronic submissions

🎯 Requirements

• University degree • Strong written and verbal English communication skills • Proficiency in R • Excellent analytical skills • Ability to successfully lead a global team • Extensive knowledge and understanding of the programming and reporting process • Knowledge of SOPs/Guidelines, ICH-GCP, and applicable local and international regulations such as 21 CFR Part 11 • Ability to learn new systems and function in an evolving technical environment • Strong project management skills • Strong organizational skills, ability to manage competing priorities, and flexibility to change • Attention to detail • Effective time management to meet daily metrics or team objectives • Business/operational skills including customer focus, commitment to quality management, and problem solving • Good presentation skills • Good business awareness/business development skills, including financial awareness

🏖️ Benefits

• Professional growth and development opportunities • Work-life balance • Flexible working hours • Collaborative and inclusive work environment

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