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 20pharmaceutical 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 800+ 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 Programmer 2 will support Emerald Clinical projects by performing statistical programming as directed by either senior management or a Emerald Clinical Statistician, take lead programmer role and mentor junior statistical programmers
Your Responsibilities
Perform, plan co-ordinate and implement the following for complex studies: o Review statistical analysis plans and mock-shells.
The programming, testing, and documentation of statistical programmes for use in creating statistical tables, figures and listings
The programming and specifications writing of SDTM datasets.
The programming and specifications writing of analysis datasets (derived datasets) and transfer files for internal and external clients
Create meta-data representations of regulatory-specific and analysis data sets.
Conduct peer-review of