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Mid Level Statistical Programmer

3+ 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

### **Mid-Level Statistical Programmer | Bangalore**  
**Job ID:** 2024-113805 | **Company:** ICON plc | **Category:** Biometrics Portfolio  

#### **About ICON plc**  
ICON plc is a **leading healthcare intelligence and clinical research organization**, advancing clinical trials from **molecule to medicine**. We support **pharmaceutical, biotechnology, and medical device companies**, as well as **government and public health organizations**, to accelerate the development of life-saving drugs and devices.  

### **Role Overview**  
As a **Statistical Programmer (ADaM)** at ICON, you will be responsible for developing and validating **safety and efficacy analysis datasets, tables, listings, and figures (TLFs)** while ensuring adherence to **CDISC** and **client-specific standards**. You will work in a **collaborative environment**, supporting clinical research teams and biostatisticians to deliver high-quality programming solutions.  

### **Key Responsibilities**  
- Develop and **validate ADaM datasets** for **safety and efficacy domains**.  
- Create and validate **safety and efficacy tables, listings, and figures (TLFs)** with accuracy.  
- Develop **study-specific or general macros** and finalize **programming specifications/mock-ups**.  
- Maintain **compliance with programming specifications** and complete necessary documentation.  
- **Plan and manage workload** effectively to meet project timelines.  
- Troubleshoot **programming issues** and ensure timely resolution.  
- Collaborate with **biostatistics, senior programming teams, and sponsors** to meet study objectives.  
- Work both **independently and within a team**, demonstrating strong **problem-solving and organizational skills**.  

### **Who You Are**  
#### **Required Qualifications**  
- **3+ years of experience** in **ADaM programming**.  
- Expertise in **creating and validating safety and efficacy TLFs**.  
- Experience in developing **ADaM datasets** for **safety and efficacy domains**.  
- Proficiency in **SAS programming** (Base SAS, PROC SQL, SAS/Stat, SAS Macros, and SAS/Graph).  
- Strong **attention to detail, communication skills**, and ability to work in **remote or hybrid teams**.  

### **Why Join ICON?**  
At **ICON**, we invest in our people through:  
✅ **Comprehensive benefits package** supporting employees and their families.  
✅ **Continuous learning culture** with engaging and challenging work.  
✅ **Competitive compensation and rewards programs**.  
✅ **Equal opportunity workplace**, fostering diversity and inclusion.  

🚀 **Apply today to be part of ICON’s mission to drive clinical research forward!**