Who We Are

Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.

With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.

Global Expertise. Local Insight. Real Impact.

Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.

Our 1000+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

The Statistical Programmers (SPs) are responsible to apply industry and regulatory standards to create and maintain standardized databases for clinical trial data. They are also responsible to provide statistical programming support for the implementation of data models and the reporting of clinical trials. They develop and perform quality control on tabulation datasets, analysis datasets and tables, figures and listings via an appropriate statistical analysis system (i.e. SAS®). They provide input to statistical analysis plan, table shells, data integration plan, and publications. They also liaise with other departments to properly implement data models (e.g. SDTM/ADaM). They research new technologies and techniques to improve efficiency of programming datasets/outputs.

Responsibilities

• Programs tabulation datasets and statistical analyses (via analysis datasets, tables, figures, listings, etc.) using appropriate statistical analysis systems (i.e. SAS®).
• Serves as a key member of project team by attending team meetings and working with biostatistician data managers and project managers.
• Performs qualify review of tabulation datasets, analysis datasets and TFL programs developed by other programmers and biostatisticians.
• Performs programming using techniques such as macro language, advanced data manipulation and statistical procedures.

About You

Bachelor’s degree in a quantitative or scientific field. Advanced degree preferred. At least 2 years of statistical programming experience. Demonstrates knowledge of computer programming, statistical analysis systems (SAS), and other procedural languages. Understands clinical informatics procedures, workflows and software systems. Displays ability to manage extremely large datasets for statistical analysis and mathematical model creation. Exhibits excellent written and oral communication skills. Demonstrates a good understanding of tabulation and analysis data structure standards (SDTM, ADaM). Demonstrates leadership skills in the coordination of statistical programming projects.

Why Join Us?

At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.

Here’s what makes us stand out:

• Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.

What We Offer

We understand that great work happens when people feel valued and supported. That’s why we provide:

• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.

Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.

We are an equal-opportunity employer and encourage applications from all qualified candidates.