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Clinical Research Physician

3+ years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Full Time Education: MD 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

### **Clinical Research Physician | Chennai**  
**Job ID:** JR125847 | **Company:** ICON plc | **Category:** Clinical Research | **Location:** Chennai (Office-Based)  

#### **About ICON plc**  
ICON plc is a **global leader in healthcare intelligence and clinical research**. We foster an **inclusive and innovative** work environment, driving excellence in **clinical development**. Join us in shaping the future of **clinical research and patient care**.  

📍 **Location:** Chennai (Office-Based)  

### **Role Overview**  
As a **Clinical Research Physician**, you will play a crucial role in **leading clinical trials**, ensuring compliance with **ethical, scientific, and regulatory** standards. You will provide **medical expertise** to advance innovative therapies while prioritizing **patient safety and trial integrity**.  

### **Key Responsibilities**  
- **Lead the design and execution** of clinical trial protocols, ensuring alignment with scientific and regulatory standards.  
- **Monitor patient safety** and oversee clinical aspects of trials, ensuring compliance with **Good Clinical Practice (GCP)**.  
- **Analyze study data and provide medical insights** to support decision-making in cross-functional teams.  
- **Engage with investigators and study sites** to ensure proper trial execution and protocol adherence.  
- **Contribute to regulatory submissions and clinical study reports** for ongoing trials.  

### **Who You Are**  
#### **Required Qualifications**  
- **Medical Degree (MD or equivalent)** with relevant experience in **clinical research**.  
- Strong understanding of **clinical trial processes and regulatory requirements**.  
- Excellent **clinical assessment skills** with a commitment to **patient safety and ethical research**.  
- Effective **communication and interpersonal skills** to engage with stakeholders.  
- Ability to **work collaboratively** in a fast-paced, team-driven environment.  

### **Why Join ICON?**  
At **ICON**, we value our people and offer:  
✅ **Competitive salary and benefits**.  
✅ **Annual leave entitlements**.  
✅ **Comprehensive health insurance** for employees and families.  
✅ **Retirement planning options** for long-term financial security.  
✅ **Global Employee Assistance Programme** for 24/7 well-being support.  
✅ **Work-life balance perks**, including gym memberships, travel subsidies, and more.  
✅ **A diverse, inclusive, and innovative work culture**.  

🌎 **Apply now and be part of ICON’s mission to advance clinical research and improve global healthcare!**