Senior Medical Writer, Taiwan

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 areembedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.

About the Role

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. May serve as primary technical contact with client.

Your Responsibilities

• Acts as Lead Medical Writer on the most complex projects (e.g., regulatory submissions, CTD modules, clinical overviews).

• Independently liaises directly with customers on medical writing issues.

• Proposes costings for less routine projects, out-of-scope activities, and potential budget efficiencies with manager guidance.

• May present on project-specific MW proposals at full-service bid defence meetings, with management input to slides as required.

• Interprets non-clinical and clinical data in the preparation of various technical reports.

• Provides senior review and guidance for most documents prepared by junior staff.

• Designs training materials; inputs into generic training plans; may deliver general Medical Writing training to internal and external groups.

• May act as Project Manager for a small series of stand-alone Medical Writing projects (e.g., series of related CSRs).

• Keeps abreast of current data, trends, medical writing/regulatory knowledge, developments and advances in drug development/medical writing.

• May propose revisions to SOPs or suggest process improvements; may draft new MW SOPs for review; acts as reviewer for MW SOPs as assigned.

About You

• A post graduate degree from an accredited institution in Life Sciences or Health-related Sciences, or equivalent.

• 5-6 years of science or medical related writing experience.

• Mastery of medical terminology and multiple therapeutic areas; able to guide others.

• Proficient in document management systems, authoring tools, and collaboration platforms.

• Excellent written, oral communication and presentation skills; able to lead client communications.

• Fluent in English reading, writing, and speaking; able to author highest complexity English regulatory documents.

• 5–8 years of experience in pharmaceutical company or CRO developing drugs for human use, including complex clinical trials and submission projects.

• Extensive experience in clinical study design and protocol development/writing; led pivotal trial (e.g., Phase III) protocols.

• In-depth knowledge of regulatory submission requirements and ICH guidelines; familiar with multi-regional submission strategies (FDA/NMPA).

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.