Medical Coding Specialist
About the role
This vacancy has now expired. Please click here to view live vacancies.
Medical Coding Specialist
Job Location: Chennai
Job Type: Permanent (Full-Time)
Summary:
An excellent opportunity to join as Medical Coding Specialist to perform medical coding of Case Report Form (CRF) terms using specified dictionary, thesauri and coding conventions to ensure coding integrity and consistency within the clinical database for specified projects.
What we do?
- Identify and apply appropriate codes from specific dictionaries to Case Report Form (CRF) terms that require manual coding (e.g. adverse events, medications/procedures, and medical conditions/history).
- Accurately and consistently apply coding conventions to Case Report Form terms in accordance with all applicable procedures.
- Review all coded terms within the clinical database for accuracy and consistency and appropriately address coding discrepancies or inconsistencies.
- Accurately generate data queries where applicable to resolve coding discrepancies.
- Maintain coding documentation within project files as appropriate.
- Perform other duties reasonably related to the position as directed by manager/designee
What you need?
- Minimum of 6 months to 1 year prior medical coding experience
- Computer, keyboarding and word processing skills as relevant to the job function.
- Thorough knowledge of standard coding dictionaries (e.g. MedDRA, WHODrug).
- Excellent understanding of medical procedures and terminology
- Ability to work within a team environment and maintain a constructive approach when responding to internal and /or external customers as required
- Professional and appropriate written and oral communication skills
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
Teaser label
Career ProgressionContent type
BlogsPublish date
11/26/2025
Summary
How Clinical Research Job Seekers Can Enhance Their Applications Finding the right role in clinical research has become increasingly competitive as organisations continue to expand their study por
Similar jobs at ICON
Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Contractor
Description
We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial
Reference
JR140062
Expiry date
01/01/0001
Author
Sophia CairnsAuthor
Sophia CairnsSalary
Location
Australia, Sydney
Department
Clinical Monitoring
Real World Solutions
Location
Sydney
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking for Clinical Site Associate to join our diverse and dynamic team. As a CSA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials,
Reference
JR140104
Expiry date
01/01/0001
Author
Krisztina AuthAuthor
Krisztina AuthSalary
Location
United States of America
Department
Clinical Monitoring
Real World Solutions
Location
Multiple US Locations
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Clinical Site Associate (CSA) Open to candidates located anywhere in the USA. We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As a CSA at ICON, you will
Reference
JR139929
Expiry date
01/01/0001
Author
Jypson Jose
Author
Jypson JoseSalary
Location
Korea, Seoul
Location
Seoul
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR138007
Expiry date
01/01/0001
Author
Sonia OhAuthor
Sonia OhSalary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
JR140203
Expiry date
01/01/0001
Author
Michal CzyrekAuthor
Michal CzyrekSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Location
Osaka
Tokyo
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
TBD
Reference
JR140195
Expiry date
01/01/0001
Author
Sachi TakamuneAuthor
Sachi Takamune