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24 days ago
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24 days ago

Medical Coder

Reading, United KingdomFull-timeRemoteMid · 2-5 yearsMedical Coder

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Must-have skills for this role

  • meddra
  • whodrug
  • medical terminology
  • medidata rave coder

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Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

About this role

Medical Coder

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


Medical Coder - Sponsor Dedicated

UK or South Africa

This position is responsible for encoding terms reported as adverse events and medical history as well as prior and concomitant medications using industry accepted dictionaries such as MedDRA and WHOdrug.

What You Will Do:

Your role will involve delivering scientific operations work to a high standard, working closely with your team and stakeholders.

Key Responsibilities:

  • Coding performed in accordance with departmental coding conventions and company SOPs. 
  • The coder will generate queries for clarification of potentially discrepant data.
  • Ability to work in cross-functional team-oriented environments.
  • Assist with data coding consistency   reviews and SAE reconciliation, as needed.
  • The Coder will collaborate with medical monitors, Clinical and Data Management team members, as required, to ensure the timely processing of coding, according to project timelines. 
  • The coder should have working knowledge of coding tools (ie. Medidata RAVE Coder, TMS, Veeva, etc.)
  • Assist in interdepartmental training of new staff as needed.

Required Qualifications

  • Bachelors degree or related health science background.  
  • Commensurate experience will be considered in lieu of a 4 year degree.
  • 2+ years industry experience in pharmacovigilance, clinical research, and/or clinical data management required.
  • Experience with MedDRA and WHODD  preferred.
  • Working knowledge of  medical terminology, clinical trials & coding is essential.
  • Excellent written and oral skills and demonstrated ability to work both independently and within cross functional teams.
  • Strong attention to detail and a commitment to high quality work"

#LI-JC3

#LI-Remote


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply

Company

Icon
Reading, United Kingdom

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Icon's careers site·first seen 28 Aug 2026·last verified 8 Sept 2026·How we source jobs

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