Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

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!**