Medical Writer

🔥 3 minutes ago

🇸🇬 Singapore – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥📝 Medical Writer

👻 Ghost score 10%

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Emerald Clinical

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2000

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Emerald Clinical is a leading global clinical research organization (CRO) founded in the Asia‑Pacific region that provides end‑to‑end clinical trial services to biopharmaceutical, medical device, and diagnostic companies. With about 25 years of experience and a team of 800+ operating across 40+ locations worldwide, Emerald Clinical manages trials across all phases including registration and post‑marketing studies, and offers clinical operations, project management, and trial staffing support. The company emphasizes scientific expertise, operational excellence, and global reach to support drug and device development.

📋 Description

• Research, write, and edit clinical documents, including clinical study reports, clinical study protocols, clinical plan outlines, regulatory submission document sections, and scientific manuscripts • Apply therapeutic expertise, clinical drug development knowledge, and relevant experience to support development of drugs, biologics, devices, and other products for human use • Independently write, review, and edit routine documents such as protocols, CSRs, IBs, and scientific manuscripts • Independently interpret non-clinical and clinical data in technical reports • Perform literature searches and reviews • Participate in project teams and coordinate report specifications and data analysis • Schedule and conduct peer and team quality-control reviews for assigned projects • Review relevant documents and interact with functional leaders and project managers to understand project timelines • Provide writing support for more complex clinical documentation under appropriate departmental supervision • Perform other tasks as directed by the line manager

🎯 Requirements

• 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 • Solid background in clinical medicine or pharmaceutical sciences • Familiarity with common medical and clinical research terminology • Familiarity with ICH-GCP and key NMPA/FDA requirements • Knowledge of the full clinical trial process and basic statistical principles • Ability to independently draft moderately complex documents, including protocols, CSR drafts, and investigator brochures • Good data interpretation skills • Proficient in English and Chinese reading and writing • Fluent in English reading, writing, and speaking; able to independently draft English documents and communicate with overseas clients or colleagues • Proficient in PC-Windows and MS Word; familiar with basic document templates • Excellent written, oral communication, and presentation skills • Ability to manage timelines for 1–2 projects • 1–3 years of experience in a pharmaceutical company or CRO developing drugs for human use • Basic experience in clinical study design and protocol development/writing, including participation in protocol drafting • Basic knowledge of regulatory submission requirements and ICH CSR writing guidelines

🏖️ Benefits

• Competitive compensation: tailored salary and benefits package reflecting skills and experience • Hybrid or remote working arrangements, depending on location and role • Career growth and learning opportunities • Access to a global network of scientific leaders • Employee wellbeing programs promoting work-life balance, health, and team connection • Global engagement surveys • Recognition programs • Team-building events • Exposure to diverse international projects and clients