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

Ensure the completeness, quality and integrity of the clinical data in database by performing/overseeing/being responsible of data management documents development, database UAT, data cleaning activities and all the other related tasks on the basis of company and/or sponsor Standard Operating Procedures (SOPs).

Responsibilities

• Understand international guidelines such as ICH-GCP, local regulatory authority regulations, Company policies, Company SOPs, Work Instructions, and processes. Contribute to SOPs, processes and systems enhancements.

• Create and maintain eCRF specifications, Data Validation Plan with guidance Create and maintain DM documentation, including but not limited to Data Management Plan, eCRF completion guidelines, SAE reconciliation plan, etc. Perform database UAT and QC activities.

• Organize and perform Data Review and Query management activities Review local lab normal ranges and contact with study team if any issues Perform SAE reconciliation and External Data reconciliation Generate data status report Perform Data Quality Control Responsible for archiving of DM documentations

About You

• Bachelor’s degree in medical, Pharmacy, Biology, Biomedical or related fields.

• 2+ years of experience in Data Management in Pharma or CRO setting.

• Proficient in of Microsoft Office tools (Outlook, Word, Excel, etc.), and conferencing software like WebEx, ZOOM, Lync, etc.

• Experience in one or more EDC platforms, such as Medidata Rave, IBM Clinical, Mobile MD, etc. Good communication skills in Mandarin and English (written and verbal).

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.