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 Senior Biostatistician is responsible for global biostatistics activities. The Senior Biostatistician is responsible for the design, analysis and reporting of medical research projects conducted by the Emerald Clinical.

Your Responsibilities

· Serve as a biostatistical consultant for other members of the department and staff members from other departments within the company;

· Maintain knowledge and awareness of developments in biostatistics and clinical trial methodology, and regulatory requirements that impact on analyses.

· Represent clients at meetings with regulatory agencies or other regulatory meetings; may participate as a member of a Data and Safety Monitoring Committee;

· Participate as biostatistician on project(s) including but not limited to developing/reviewing protocols, preparing analysis plans, randomization plan, and writing sections of joint clinical/statistical reports, ISSs, ISEs and/or NDA sections, programming/ validation of TLFs and performing other relevant activities as required;

· Coordinate and support internal and contracted staff in accordance with organization’s policies and applicable regulations.

· Participate in project meetings; keep up to date on project issues;

· Coordinate and participate in process improvements and interoffice/ interdepartmental task forces; oversee collection and reporting of Biostatistics metrics, implementation of revised work practices, new guidelines, and new software tools as they become available;

· Make recommendations about resource allocation for team members to achieve target utilization rates and project realization rates;

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

· Attend and actively participate in Emerald Clinical meetings and other internal meetings and activities as required

· 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

Education and Experience

· M.Scs. or Ph.D. in Biostatistics, Maths or science related field

· Minimum 7 years’ experience in Biostatistics or related work Prior experience in the CRO environment is preferable

Competencies

· Experience in SAS Programming is an added advantage

· 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.

• 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.