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Senior Medical Writer

5+ years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Education: PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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**Senior Medical Writer – Auckland (JR121957) – senior-medical-writer-auckland**  

### **About the Role**  
Medical Writer II / Senior Medical Writer – Home-based in New Zealand. Join us and advance your career with an industry-leading CRO.  

ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence, welcoming you to join us in shaping the future of clinical development.  

At ICON, it’s our people that set us apart. Our diverse teams make us a better partner to our customers and help us fulfill our mission of advancing and improving patients’ lives.  

### **Our Culture**  
Our ‘Own It’ culture is built on four core values:  
✅ **Accountability & Delivery**  
✅ **Collaboration**  
✅ **Partnership**  
✅ **Integrity**  

We strive to be the **Clinical Research Organization of choice**, delivering excellence to both clients and patients. If you're as driven as we are, you’ll be part of a dynamic, supportive environment, surrounded by some of the best minds in the industry.  

### **The Opportunity**  
This is a rare **home-based** opportunity in New Zealand to join our **global Medical Writing team**, a key part of ICON’s Clinical Research Services group. Our team is responsible for producing high-quality documents supporting clinical studies and regulatory submissions.  

#### **Your Responsibilities**  
🔹 Writing and reviewing essential study documents (e.g., Protocol, Synopsis, Informed Consent, Data Collection Documents, Study Reports).  
🔹 Developing scientific communication materials (abstracts, posters, manuscripts, etc.).  
🔹 Performing quality control for medical writing deliverables.  
🔹 Interpreting statistical results and collaborating with statisticians to develop study reports and scientific documents.  
🔹 Participating in quality assurance improvements.  
🔹 Representing medical writing activities during bid defense presentations.  

### **What You Need to Succeed**  
✔ **Experience**: 5+ years in Medical Writing within a pharmaceutical, biotechnology, CRO, or healthcare setting.  
✔ **Education**: PhD in a **medical or biological field** (preferred).  
✔ **Knowledge**: Familiarity with **ICH/GCP guidelines** or other relevant industry standards.  
✔ **Skills**:  
- Outstanding written and verbal communication.  
- Strong computer literacy.  
- Ability to collaborate effectively with team members.  

### **Why Join ICON?**  
Our **success depends on our people**, and we prioritize building a culture that rewards high performance and nurtures talent.  

#### **Benefits at ICON:**  
💰 **Competitive Salary Packages** – Benchmarked regularly to stay competitive.  
🎯 **Performance-Based Annual Bonuses** – Rewarding both individual and company-wide success.  
🏥 **Comprehensive Health Benefits** – Coverage for employees and families.  
🏦 **Retirement Planning** – Competitive plans to help you save with confidence.  
💡 **Career Growth** – An environment that fosters learning, development, and innovation.  
🌍 **Diversity & Inclusion** – ICON is an **equal-opportunity employer**, committed to providing a discrimination-free workplace.  

#### **Interested but unsure if you meet all requirements?**  
Apply anyway! You might be exactly what we’re looking for at ICON.  

🔗 **Apply now and be part of our journey in advancing global healthcare.**  

**#LI-KA1 #LI-Remote**  

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