JUMP TO CONTENT

Senior Medical Editor

JR071818

About the role

This vacancy has now expired. Please click here to view live vacancies.

Senior Medical Editor - Medical Communications/Pubs

Homebased locations throughout the US

At ICON, it's our people that set us apart.

As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry. Are you one of them?

We are looking for conscientious, resilient, and inspiring individuals to join our team. As a Senior Medical Editor (SME), your primary responsibility will be to provide medical editing support as part of a dedicated team servicing assigned clients. Although the ability to work independently is key, the SME will work closely with their assigned client account teams to help ensure the timely delivery of high-quality and scientifically/medically accurate projects. Your participation in internal company initiatives, as required, offers additional potential opportunities for growth.

The Role

As a Senior Medical Editor, in-depth medical editing experience with a background in copyediting, proofing, fact-checking, and formatting documents such as manuscripts, abstracts, slide presentations, and posters for medical publications/communications is expected and will be an integral foundation for this role. The SME role will fall broadly across the following approximate allocations (individual client account teams may have specific needs that may alter these allocations as necessary):

  • 60% of your time will be devoted to editing, proofing, fact-checking, and formatting documents, ensuring
  • Correct grammar, punctuation, spelling, and usage according to the American Medical Association Manual of Style
  • Proper style has been followed based on company style guide, individual client style sheets, and/or journal/congress style
  • References have been edited, updated, and formatted using EndNote
  • Clarity, consistency, and accuracy of all jobs assigned
  • Author/writer changes have been correctly incorporated
  • Journal galley proofs have been accurately created from original submission document
  • 20% of your time will be devoted to creating mock submissions and supporting Library Services as needed by
  • Downloading journal/congress author guidelines in preparation for manuscript and abstract submission by client team
  • Creating mock submission documents based on journal/congress submission guidelines
  • Providing backup to Editorial Manager by ordering journal articles for writers
  • Researching journals/congresses for potential submission of client deliverables
  • Performing literature searches based on keywords and parameters provided by client teams
  • 15% of your time will be devoted to general editorial duties such as
  • Trafficking work from assigned client team
  • Training new medical editors and onboarding new scientific staff as necessary
  • Updating client style sheets and house style guide
  • Maintaining product EndNote libraries
  • Ensuring prompt communication with assigned team, Editorial Manager, and other medical editors to ensure jobs are completed within allotted time frame
  • Attending company, team, and department meetings, coming prepared to provide updates on the status of assigned work
  • 5% of your time will be devoted to company requirements such as
  • Recording all time worked in ICON time management systems
  • Maintaining goals in Performance section of Workday
  • Completing all mandatory iLearn courses and compliance training for select clients
  • Maintaining knowledge of required software (MS Office suite, Sharepoint, EndNote, Acrobat Pro, iThenticate)
  • Performing responsibilities in a professional manner, meeting company mission and goals
  • Performing any other duties as required or assigned

What you need

  • Bachelor's degree, preferably in English, Science, or Communications
  • 3 to 5 years of scientific and/or medical editing experience, ideally in the medical communications or publishing field (years of experience required are approximate and may be less or more depending on how well the editor exhibits the skills outlined)
  • Excellent verbal/written communications skills; must demonstrate a command of the English language (read, write and speak).
  • Ability to work efficiently with network directories/databases
  • Ability to prioritize and organize work, meet deadlines, multitask, and successfully function within a team setting
  • A strong desire to be a key part of a global network of services that lead to better outcomes for its clients, its people, and for patients…apply now and Own IT@ICON!

Why join us?

Ongoing development is vital to us, and as a Senior Medical Editor, you will have the opportunity to progress your career, with the potential to grow your skills in multiple areas of interest, whether that is training others, leading a task force, or developing creative solutions to improve work processes. Our benefits package is competitive, our scope is international, and we genuinely care about our people and their success.

ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.

EOE race/color/religion/sex/sexual orientation/gender identity/disability/vet/national origin

List #1

Day in the life

Two computer monitors with data graphs
How Data Moves Through a Clinical Trial

Teaser label

Industry

Content type

Blogs

Publish 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

Discover how data flows through a clinical trial and learn where your skills could fit within clinical research.

Read more
Male and female auditing a manufacturing facility
Quality and Compliance - A Plain Language Guide

Teaser label

Industry

Content type

Blogs

Publish 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

A clear, practical introduction to quality and compliance for those starting a career in clinical research.

Read more
Female using a laptop to search for jobs
Improving Your Visibility in the Clinical Research Job Market

Teaser label

Career Progression

Content type

Blogs

Publish 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

Teaser label

Discover the search terms recruiters use most often and practical steps that can help candidates strengthen their visibility.

Read more
View all

Similar jobs at ICON

Clinical Research Associate

Salary

Location

Romania, Bucharest

Location

Bucharest

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking experienced Clinical Research Associates with previous experience in oncology to join our diverse and dynamic FSP team in Romania.As a Clinical Research Associate at ICON Plc,

Reference

JR139956

Expiry date

01/01/0001

Dariusz Sternlicht Read more Shortlist Save this role
Clinical Site Associate

Salary

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

Jypson Jose

Author

Jypson Jose
Jypson Jose

Author

Jypson Jose
Read more Shortlist Save this role
Senior Manager, Regulatory Affairs - IVD

Salary

Location

Regional United States (PRA)

Location

Multiple US Locations

Portland

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug / Device Regulatory Affairs

Job Type

Permanent

Description

Sr Manager, Regulatory Affairs – IVDLocation: US Remote, Portland, OR area preferredWe are currently seeking a Senior Manager, Regulatory Affairs to join our diverse and dynamic team. As a Senior Mana

Reference

JR137759

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role
Clinical Quality Compliance Lead

Salary

Location

US, Blue Bell (ICON)

Department

Full Service - Development & Commercialisation Solutions

Location

Dublin

Blue Bell

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Quality Assurance

Job Type

Permanent

Description

We are currently seeking a Clinical Quality Compliance Lead to join our diverse and dynamic team. As a Clinical Quality Compliance Lead at ICON, you will play a pivotal role in designing and analyzing

Reference

JR136890

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role
Manager, Business Continuity

Salary

Location

Poland, Warsaw

Department

Full Service - Corporate Support

Location

Mexico City

Sofia

Dublin

Warsaw

Bangalore

Chennai

Trivandrum

Bengaluru

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Facilities & Administratives Services

Job Type

Permanent

Description

Role Overview We are seeking a highly skilled Manager, Business Continuity to join our team and help ensure ICON is prepared to respond effectively to business interruptions. You will collaborate with

Reference

JR137815

Expiry date

01/01/0001

Magda Kozuszek Read more Shortlist Save this role
Clinical Research Coordinator

Salary

Location

US, Wilmington, NC

Department

Accellacare Site Network

Location

Wilmington

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Research Site Services

Job Type

Permanent

Description

We are currently seeking a Clinical Research Coordinator (CRC) to join our diverse and dynamic team. As a CRC Level 1 at ICON, you will play a pivotal role in designing and analyzing clinical trials,

Reference

JR136997

Expiry date

01/01/0001

Sasha Brown

Author

Sasha Brown
Sasha Brown

Author

Sasha Brown
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above