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Senior Cdc

3-5 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

### **Senior CDC | Bangalore**  
**Job ID:** 2025-116385 | **Company:** ICON plc | **Category:** Biometrics Portfolio  

#### **About ICON plc**  
ICON plc is the **world’s largest and most comprehensive clinical research organization**, powered by **healthcare intelligence**. We advance clinical trials through innovative solutions that accelerate the development of life-saving therapies.  

### **Role Overview**  
As a **Senior CDC (Clinical Data Coordinator II)**, you will play a key role in managing **clinical data standards, metadata, and documentation**, ensuring high-quality data collection and processing. This role is **specific to the COMPASS system** and requires **3-5 years of experience** in a similar capacity.  

📍 **Location:** Chennai (Office-Based) | **Immediate Joiners Only**  

### **Key Responsibilities**  
- **Communicate with cross-functional teams** (Clinical Programming, CDSP, CDM) to ensure seamless progress.  
- Manage **study-specific documentation** and review **guidance documents**.  
- Participate in **CDSP meetings** and manage configuration timelines.  
- Handle **metadata creation and updates** for standards and studies.  
- Update metadata for **protocol amendments and post-go-live EDC/DTS changes**.  
- Understand and work with **elluminate validator, standards, and metadata functionalities**.  

### **Who You Are**  
#### **Required Qualifications**  
- **3-5 years of experience** in clinical data coordination.  
- **Experience working with COMPASS** is mandatory.  
- Strong skills in **metadata management** and **clinical data documentation**.  
- Ability to work in a **fast-paced, collaborative environment**.  

### **Why Join ICON?**  
At **ICON**, we prioritize a culture that fosters **high performance and talent development**, offering:  
✅ **Competitive salary and benefits package**.  
✅ **Annual leave entitlements** to promote work-life balance.  
✅ **Health insurance plans** tailored to your needs.  
✅ **Retirement planning options** for financial security.  
✅ **Global Employee Assistance Programme** (TELUS Health) for well-being support.  
✅ **Diversity & Inclusion** commitment—creating a workplace where **everyone belongs**.  

🌎 **Apply today and be part of ICON’s mission to transform clinical research!**