Company Overview
ICON plc is a world-leading healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, medical device, and public health organizations in advancing clinical development and improving patient outcomes.
Job Details
|
Category |
Details |
|---|---|
|
Job Title |
Manager, Statistical Programming |
|
Company |
ICON plc |
|
Department |
Statistical Programming / Biostatistics |
|
Industry |
Clinical Research / Pharmaceutical / Biotechnology |
|
Employment Type |
Full-Time |
|
Education Required |
Bachelor’s Degree |
|
Preferred Fields |
Statistics, Computer Science, Mathematics, or Related Discipline |
|
Experience Level |
Managerial / Senior-Level |
Role Summary
The Manager, Statistical Programming is responsible for leading statistical programming activities for clinical trials, including development and validation of datasets, statistical analyses, and reporting outputs. The role involves managing a team of statistical programmers, ensuring high-quality deliverables, regulatory compliance, and alignment with study objectives and timelines.
The position also focuses on mentoring team members, improving operational efficiency, and maintaining best practices in statistical programming.
Key Responsibilities
1. Statistical Programming Leadership
Lead day-to-day statistical programming activities.
Oversee programming deliverables for clinical trial studies.
Ensure timely and high-quality project execution.
2. Clinical Trial Programming
Manage programming activities related to:
Clinical trial datasets
Statistical Analysis Plans (SAPs)
Tables, Listings, and Figures (TLFs)
Support accurate analysis and reporting of clinical trial data.
3. Team Management & Mentorship
Manage and mentor statistical programming teams.
Foster a collaborative and high-performing work environment.
Support professional development and technical growth of team members.
4. Cross-Functional Collaboration
Collaborate with:
Biostatisticians
Clinical teams
Project stakeholders
Ensure programming activities align with:
Study objectives
Project timelines
Regulatory expectations
5. Quality Review & Compliance
Review and validate programming outputs.
Ensure compliance with:
Regulatory standards
Internal quality procedures
Industry best practices
Maintain accuracy and consistency of deliverables.
6. Process Improvement & Innovation
Stay updated on:
Statistical programming technologies
Industry best practices
Emerging tools and techniques
Drive improvements in:
Programming efficiency
Data quality
Operational processes
Required Qualifications
Educational Requirements
Bachelor’s Degree in:
Statistics
Computer Science
Mathematics
Related discipline
Experience Requirements
Extensive experience in:
Statistical programming
Clinical research
Pharmaceutical or biotechnology environments
Experience managing programming teams and project deliverables.
Technical Skills
Programming Languages
SAS
R
Expertise Areas
Statistical Analysis Plans (SAPs)
Clinical trial datasets
TLF generation
Clinical data analysis
Statistical reporting
Data validation
Leadership & Functional Skills
Team leadership and people management
Project coordination
Regulatory compliance knowledge
Problem-solving and analytical thinking
Quality-focused mindset
Continuous improvement orientation
Soft Skills
Strong communication abilities
Ability to explain complex statistical concepts
Stakeholder collaboration
Organizational and multitasking skills
Strategic thinking and decision-making
Preferred Candidate Profile
Ideal candidates may have experience in:
Clinical Trial Programming
Biostatistics
SDTM/ADaM standards
TLF development
Regulatory submissions
Clinical data reporting
CRO environments
Pharmaceutical or Biotechnology industries
Statistical programming leadership
Benefits Offered
Compensation & Rewards
Competitive salary package
Recognition and performance programs
Health & Wellbeing
Comprehensive health insurance options
Employee Assistance Programme (TELUS Health)
Life assurance coverage
Wellness initiatives
Work-Life Balance
Annual leave entitlements
Flexible employee benefits
Family-focused support policies
Financial & Lifestyle Benefits
Retirement planning programs
Childcare vouchers
Bike purchase schemes
Discounted gym memberships
Subsidized travel passes
Health assessments
Diversity & Inclusion
ICON plc is committed to maintaining an inclusive and accessible workplace and provides equal employment opportunities regardless of:
Race
Religion
Gender
Sexual orientation
Gender identity
National origin
Disability
Veteran status
Reasonable accommodations are available during the recruitment and employment process.
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Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
Atlanta | Augusta | Rome |Maine :
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Mexico |northeastern :
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Budapest |BULGARIA :
Bulgaria | Vedant |Denmark :
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Finland |Istanbul :
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Norway | NOrway |Romania :
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Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Sheffield |Oxfordshire :
Witney |Ontario :
Richmond Hill | North York | Australia | Renfrew | Uxbridge | Mississauga |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
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Auckland |New Zealand :
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Vienna |Catalonia :
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Cebu City |Philippines :
Manila |Croatia :
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Hanoi | Hà Nội |Ho Chi Minh :
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Rho |Jakarta :
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Japan | Saitama |Tokyo :
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Sofia |Sweden :
Sweden |Taipei :
Taipei |Mazovia :
Warsaw |
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