Senior Statistical Programmer (R) - Remote with Impact

ICON Strategic Solutions; Philippines; On-site; PHP 1,674,000 - 3,013,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life insurance

Flexible country-specific benefits

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization offering a homebased Senior Statistical Programmer role. You will analyze clinical trial data, develop SAS programs, and collaborate with biostatisticians to define analyses.

The position emphasizes quality, QC checks, and regulatory reporting. You should have a strong foundation in statistical programming, with at least 3 years in the field and the ability to work independently from a home-based setup.

Qualifications

• Bachelor's degree in statistics or related discipline.
• 3+ years of experience in statistical programming.
• Proficiency in SAS programming; experience with R in clinical studies is a plus.
• Excellent analytical and problem-solving skills.
• Strong communication and teamwork abilities.
• Must be amenable to a home-based setup.

Responsibilities

• Lead statistical programming tasks with emphasis on quality and improvements.
• Develop and validate SAS programs for analysis and reporting of trial data.
• Collaborate with biostatisticians to define analysis plans.
• Perform QC checks on outputs and ensure reporting accuracy.
• Assist in preparing statistical reports for regulatory submissions.
• Identify efficiencies and contribute to programming process improvements.

Skills

R programming

Statistical analysis

Analytical thinking

Communication skills

Team collaboration

Attention to detail

Home-based work readiness

Education

Bachelor's degree in statistics or related discipline

Tools

SAS programming

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organization offering a homebased Senior Statistical Programmer role. You will analyze clinical trial data, develop SAS programs, and collaborate with biostatisticians to define analyses.

The position emphasizes quality, QC checks, and regulatory reporting. You should have a strong foundation in statistical programming, with at least 3 years in the field and the ability to work independently from a home-based setup.