Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 pharmaceutical 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.
Researches, writes, and edits clinical documents, including clinical study reports, clinical study protocols, clinical plan outlines, sections of regulatory submission documents, and scientific manuscripts by applying therapeutic expertise and clinical drug development knowledge and relevant experience to the development of drugs, biologics, devices and or other products for human use. May provide writing support for more complex clinical documentation, with appropriate departmental supervision.
Independently writes, reviews, and edits routine documents (e.g., protocols, CSRs, IBs, scientific manuscripts).
Independently interprets non-clinical and clinical data in preparing technical reports.
Independently performs literature searches and reviews.
Participates in project teams, coordinating report specifications and data analysis.
Schedules and conducts peer and team quality control reviews for assigned projects.
Reviews relevant documents and interacts with functional leader and project manager to understand project timelines.
Performs other tasks as directed by line manager.
Knowledge: Solid background in clinical medicine or pharmaceutical sciences; familiar with ICH-GCP and key NMPA/FDA requirements; knowledge of full clinical trial process and basic statistical principles.
Skills: Independently drafts moderately complex documents (protocols, CSR drafts, IB); good data interpretation skills; proficient in English and Chinese (reading and writing).
Abilities: Good cross-functional communication skills; ability to manage timelines for 1–2 projects; problem-solving awareness.
Bachelor's/Master's degree from an accredited institution in Life Sciences or Health-related Sciences.
2-4 years of science or medical related writing experience.
Familiar with common medical terminology and clinical research terminology.
Proficient in PC-Windows and MS Word; familiar with basic document templates.
Excellent written, oral communication and presentation skills; able to participate in project team communications.
Fluent in English reading, writing, and speaking; able to independently draft English documents.
1-3 years of experience in pharmaceutical company or CRO developing drugs for human use (e.g., medical writing, clinical trial management).
Basic experience in clinical study design and protocol development/writing (participated in protocol drafting).
Basic knowledge of regulatory submission requirements and ICH CSR writing guidelines.
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.
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.
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