Statistical Programmer 1

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 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 Programmer 1 will support Emerald Clinical projects by performing statistical programming as directed by either senior management or an Emerald Clinical Statistician.

Responsibilities

• Perform, plan, co-ordinate, and implement the following for complex studies:

Ø The programming, testing, and documentation of statistical programmes for use

Ø in creating statistical tables, figures, and listings.

Ø The programming and specifications writing of SDTM datasets

Ø The programming of analysis datasets (derived datasets) and transfer files for

Ø internal and external clients.

Ø The programming quality control checks for the source data and report the data

Ø issues periodically.

• Directly communicate with internal team including data management, project

management, and client statisticians and client team members to ensure

appropriate understanding of requirements and project timelines.

• Use and promote the use of established standards, SOP, and best practice

Training, Quality and Compliance

• Complete mandatory training for this role within specified timelines

• Attend mandatory training sessions required for this role

• Identify resources and training to support learning and development within this role

• Comply with all applicable regulations, guidelines, SOPs, and project-specific

requirements

• Comply with all designated systems relevant to this role

• Ensure own quality control of all relevant processes and activities performed

• Report and escalate identified risks and issues in areas of responsibility according

to Emerald Clinical and/or project requirements

Customer Focus and Teamwork

• Provide input to systems, tools, and processes to support continuous improvement

Share knowledge with others, to facilitate learning and development across the organization

Work Health and Safety

• Comply with Work Health & Safety (WH&S) legislation and operate in accordance

with established organisational WH&S practice and procedures

• Promote and contribute to a safe, secure environment for staff and visitors

About You

• Minimum Bachelor of Science (BSc) degree

• Completed SAS certification • Minimum 1 years’ experience with statistical programming in SAS • Minimum 2 years’ experience in the CRO environment

Competencies

• Technological proficiency including SAS

• Ability and motivated to learn and develop • Good teamwork and willing to help other team members

• Technological proficiency including Microsoft Office packages

• Ability to see the big picture, yet still focus on detail and quality of work

• Ability to be flexible and adaptable in the face of changing organisational priorities and ambiguous environments

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.