📈 Drive Data Excellence as Statistical Programmer II
Join Emerald Clinical as a Statistical Programmer II and play a pivotal role in transforming clinical data into meaningful insights that advance medical research. This position offers the opportunity to lead programming activities, mentor junior team members, and contribute to groundbreaking clinical trials in renal, cardiometabolic, and oncology therapeutic areas.
🎯 Your Impact: Key Responsibilities
Statistical Programming Leadership
- Perform, plan, coordinate, and implement statistical programming for complex studies
- Review statistical analysis plans and mock-shells to ensure optimal study design
- Program, test, and document statistical programs for creating tables, figures, and listings
- Develop SDTM datasets and analysis datasets with comprehensive specifications
Technical Expertise & Project Management
- Provide advanced technical expertise for internal and external clients on complex studies
- Serve as technical team lead for single complex studies or groups of studies
- Directly communicate with data management, project management, and client statisticians
- Estimate programming scope, manage resources, and negotiate project timelines
Quality Control & Mentorship
- Conduct peer reviews of outputs from junior statistical programmers
- Program quality control checks for source data and report issues periodically
- Create meta-data representations of regulatory-specific and analysis datasets
- Mentor and support the development of junior statistical programming staff
Compliance & Standards Implementation
- Use and promote established standards, SOPs, and best practices
- Ensure quality control of all relevant processes and activities
- Report and escalate identified risks according to project requirements
- Maintain compliance with all designated systems and training requirements
⭐ Your Profile: Qualifications & Experience
Essential Requirements
- Minimum BS degree in sciences related field
- 3+ years experience with statistical programming in SAS
- 3+ years experience in CRO environment
- Technological proficiency in SAS and Microsoft Office
Technical Competencies
- Strong expertise in SDTM dataset programming and specifications
- Experience creating analysis datasets and transfer files
- Knowledge of statistical analysis plans and mock-shell development
- Understanding of regulatory requirements for clinical data
Professional Attributes
- Ability to see the big picture while maintaining attention to detail
- Flexibility and adaptability in changing organizational priorities
- Strong team player willing to help other team members
- Motivated to learn and develop, with commitment to knowledge sharing
Additional Requirements
- Willingness to travel as needed for project requirements
- Ability to work effectively in ambiguous environments
- Commitment to quality and compliance standards
💫 Why Join Emerald Clinical?
Purpose-Driven Impact
- Contribute to clinical trials that improve lives in renal, cardiometabolic, and oncology
- Work with a global CRO with rich Asia-Pacific heritage and local expertise
- Support diverse patient recruitment and meaningful community engagement
- Help bring innovative therapies to patients in need worldwide
Professional Growth & Development
- Clear pathway to senior programming and leadership roles
- Access to global network of scientific leaders and learning opportunities
- Mentorship from experienced statistical programming professionals
- Exposure to diverse therapeutic areas and complex study designs
Flexible Work Environment
- Hybrid or remote working arrangements based on location and role
- Support for work-life balance and employee wellbeing
- Modern technology infrastructure and programming tools
- Collaborative culture that values diverse perspectives
Global Opportunities
- International reach with exposure to diverse projects and clients
- Participation in global engagement surveys and recognition programs
- Team-building events and professional networking opportunities
- Cross-cultural collaboration and knowledge sharing
Comprehensive Benefits
- Competitive compensation package tailored to skills and experience
- Health and wellness programs promoting work-life balance
- Professional development and training support
- Global team connection initiatives and events
✨ Ready to Advance Clinical Research Through Data Excellence?
If you're an experienced statistical programmer with SAS expertise and passion for clinical research, we encourage you to apply. This Statistical Programmer II role offers the perfect opportunity to grow your career while contributing to meaningful clinical trials that address critical health challenges worldwide.
Apply Now & Help Us Improve Health for Millions Worldwide!
We are an equal opportunity employer committed to creating a diverse and inclusive workplace. We welcome applications from all qualified candidates regardless of background or experience level.
