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 Clinical Research Associate 2 is a member of the Clinical Operations group at Emerald Clinical. The Clinical Operations group is responsible for site management, monitoring tasks, and the operational support of clinical trials. The group allocates resources to projects as appropriate to assist with implementing project plans and to ensure compliance with regulatory requirements and Standard Operating Procedures (SOPs)

Your Responsibilities

• Develops statistical analysis plans and reporting specifications for simple to moderate clinical studies.

• Develops and describes appropriate statistical techniques for the analysis of data in a statistical analysis plan.

• Works with other statisticians on statistical methodology, study design, therapeutic area details, and data analysis.

• Design appropriate shells and specifications for outputs.

• Performs statistical analyses and interprets results for simple to moderate clinical studies.

• Develops or QCs analysis programs to implement techniques described in the statistical analysis plan.

• Approves final database for freeze/lock.

• Assesses model assumptions for statistical analyses.

• Works with programmers, writers, and clinicians to coordinate data summarization and analysis activities, including summary statistics, tabulations, graphics, analysis output, and raw data listings.

• Develops statistical reports and statistical sections of clinical study reports.

• Contributes statistical expertise to project teams for the design, analysis, and reporting of simple to moderate clinical studies.

• Serves as primary functional representative on project teams.

• Provides input into the preparation and review of clinical study protocols.

• Creates dummy and final randomization schemes for clinical studies.

• Participates in the development and review of CRFs, data edit specifications, and critical variable lists.

• Works with the project manager and functional manager to determine resource projections and project schedules.

• Visits clients to discuss statistical issues.

• Maintains, develops, and shares knowledge of company and industry procedures and methodologies.

• Performs billable work in accordance with WuXi CDS’s policies, procedures, and SOPs.

• Maintains solid knowledge of drug development process.

• Maintains solid knowledge of SAS procedures and good programming practices.

• Continues statistical training on new methods and techniques via self-study, internal training and courses, and external conferences and courses.

• Develops knowledge of FDA and EMEA guidelines and requirements for reporting of clinical trials data.
  

About You

• MS degree with 3 years of experience or PhD degree in statistics or biostatistics with 2 years of experience

• Demonstrated expertise in multiple statistical areas

• Demonstrated ability to plan, implement, and monitor the statistical processes for clinical studies

• Excellent written and oral communication skills; Read, write and speak English.

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.