What does a Statistical Programmer do?

Explore the responsibilities, collaboration, and growth opportunities of a Statistical Programmer in the Clinical Research Industry

Statistical Programmers at Parexel play a crucial role in analyzing and reporting clinical study data. They leverage their expertise in SAS programming and statistical analysis to support the development of life-changing treatments. By ensuring data quality and regulatory compliance, Statistical Programmers contribute significantly to Parexel's mission of accelerating the delivery of new therapies to patients.

Browse our open Statistical Programmer positions or learn more about a day in the life of a Statistical Programmer.

Q: What are the job responsibilities of a Statistical Programmer?

A: Statistical Programmers at Parexel are responsible for:

• Producing and quality-checking derived datasets (e.g., SDTM, ADaM), tables, figures, and data listings

• Developing efficient SAS programs for data analysis and reporting

• Reviewing statistical analysis plans and mock-shells

• Coordinating project start-up activities and creating global programs

• Ensuring compliance with SOPs, ICH-GCP, and other regulatory requirements

• Participating in quality control processes for all programming activities

• Collaborating with cross-functional teams to resolve programming issues

• Maintaining supporting documentation for studies to ensure traceability

• Contributing to process and quality improvement initiatives

• Providing technical expertise and consultancy on statistical programming tasks

• Staying updated on industry technical standards (e.g., CDISC, 21 CFR Part 11)

• Mentoring junior team members and providing relevant training

Q: What career progression is typical for a Statistical Programmer?

A: A typical career progression for a Statistical Programmer at Parexel may include:

• Associate Statistical Programmer: Entry-level position focusing on basic programming tasks
• Statistical Programmer: Increased responsibilities in data analysis and project involvement
• Senior Statistical Programmer: Leading programming components of projects and mentoring junior staff
• Principal Statistical Programmer: Overseeing multiple projects and contributing to strategic decisions
• Statistical Programming Manager: Managing teams and involved in high-level client interactions
• Director of Statistical Programming: Shaping department strategy and contributing to business development

Parexel offers various growth opportunities through:

• On-the-job training and mentorship 

• Exposure to diverse therapeutic areas and study types

• Opportunities to lead projects and teams

• Continuous learning in regulatory requirements and industry standards

• Participation in process improvement initiatives

• Potential for cross-functional experiences

Q: Which roles do I collaborate with as a Statistical Programmer?

A: As a Statistical Programmer at Parexel, you will collaborate with various roles across the organization, including:

• Data Managers

• Clinical Research Associates (CRAs)

• Medical Writers

• Project Managers

• Regulatory Affairs Specialists

• Quality Assurance Professionals

• Clinical Trial Managers

• Database Programmers

• Client Representatives

• Other Statistical Programmers

This cross-functional collaboration ensures comprehensive and accurate data analysis and reporting throughout the clinical research process.

Q: How does a Statistical Programmer in clinical research differ from other industries?

A: Statistical Programmers in clinical research, particularly at Parexel, differ from those in other industries in several key ways:

• Regulatory focus: They must adhere to strict guidelines set by regulatory bodies like the FDA and EMA
• Patient impact: Their work directly contributes to the development and safety of medical treatments
• Specialized data standards: They work with industry-specific standards like CDISC, SDTM, and ADaM
• Clinical trial expertise: They need to understand the complexities of clinical trial design and execution
• Therapeutic area knowledge: They often work across various medical fields, requiring broad scientific understanding
• Pharmacovigilance considerations: They may be involved in safety reporting and analysis
• Global perspective: They often work on international studies requiring knowledge of various regulatory environments
• Ethical considerations: They must maintain high ethical standards due to the sensitive nature of clinical data
• Cross-functional collaboration: They work closely with diverse teams of scientists, clinicians, and regulatory experts

Q: Will I have to travel as a Statistical Programmer?

A: Travel requirements for Statistical Programmers at Parexel are generally minimal. Most of the work can be done remotely or from a local office. However, some travel may occasionally be necessary for:

Attending key client meetings or bid defenses
Participating in important internal team discussions
Representing Parexel at industry conferences or events
Attending training sessions or workshops

The extent of travel can vary depending on the specific role, project requirements, and career level. Parexel strives to maintain a good work-life balance and leverages technology to minimize unnecessary travel.

Q: Are there remote job opportunities as a Statistical Programmer?

A: Yes, Parexel offers remote job opportunities for Statistical Programmers. The company recognizes the importance of work-life balance and flexibility, which is why they provide remote work options. As a Statistical Programmer, you can:

• Work remotely on most day-to-day tasks

• Collaborate with virtual teams using advanced communication tools

• Participate in global projects from your home office

• Benefit from Parexel's supportive remote work culture

While some occasional in-person meetings may be required, Parexel strives to accommodate remote work arrangements, allowing Statistical Programmers to maintain a healthy work-life balance while contributing to critical clinical research projects.