At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from registration to post-marketing.

Our therapeutic expertise spans renal, cardiometabolic, and oncology—areas where we make a significant impact on improving global health.

At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need.

About the Role

The Senior Statistical Programmer will support Clinical projects by performing statistical programming as directed by either senior management or Clinical Statistician, take lead programmer role and mentor junior statistical programmers.

Your Responsibilities

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

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 including efficacy datasets) and transfer files for internal and external clients o Create meta-data representations of regulatory-specific and analysis data sets.

Conduct peer-review of outputs from junior statistical programmers.

The programming quality control checks for the source data and report the data issues periodically o Randomisation list generation

Provide advanced technical expertise in conjunction with internal and external clients and independently bring project solutions to SP teams and Statistical Programming department, for complex studies. Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.

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.

Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables. • Participating in RFPs and bid defense meetings.

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

Training, Quality and Compliance Senior Statistical_Programmer_

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 Clinical and/or project requirement

About You

Minimum BS degree in sciences related field.

Minimum 6 years’ experience with statistical programming in SAS.

Minimum 6 years’ experience in the CRO environment.

Technological proficiency in SAS Competencies

Ability and motivated to learn and develop, including sharing knowledge with others

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 organizational 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.