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Medical Writer I - Medical Communications

JR063819

About the role

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

We are looking for a Medical Writer to join our winning team rated by Forbes as one of America's best large employers in 2019.

This is an exciting opportunity to work within a fast-paced environment with a team committed to being the best strategic medical communications agency in the world by leading the industry in quality, service, and innovation. At CHC Group, our value is our people, who consistently deliver the highest-quality work to our clients.

As a Medical Writer, you will provide medical/clinical writing support for as part of a dedicated team servicing a particular pharmaceutical client. This includes development of outlines, manuscripts, abstracts, scientific posters, and slide presentations that are generally focused on a specific therapeutic area. The Senior Medical Writer works closely with other Editorial and Client Services team members to meet client expectations, budgets and timelines. Travel to professional meetings, client locations, and other project-related travel may be required.

Who Are We?

Through the recent acquisition of CHC Group and MediMedia Managed Markets (MMMM) LLC, ICON plc has strengthened its expertise in scientific communications and market access. ICON is a fast-growing global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries, known for its innovative approach. ICON's core commercialization and outcomes capabilities coupled with the strategic consultancy services of CHC Group and MMMM, has created the industry's most integrated product development, clinical communication and market access solution. This means more growth and career opportunities for our current and future employees!

What's In It For You?

We provide our Medical Writers with a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.

We have a friendly environment where you can be fully engaged, motivated and rewarded. We allow you to shine because it enables us to achieve our goals. Our employees are our best asset and we encourage upward mobility by enabling them to realize their potential within a performance culture that is demanding and exciting.

To Succeed You Will Need:

  • You must have an advanced science degree (PharmD, PhD or MD, etc)
  • Excellent demonstrable understanding of ICMJE and GPP guidelines and regulations required.
  • Ability to read, analyze, and interpret common scientific and technical journals.
  • Ability to respond to common inquiries or complaints from customers.
  • Ability to write presentations and articles for peer reviewed publications that conform to prescribed style and format.
  • Must demonstrate a command of the English language (read, write and speak).
  • Ability to work with mathematical concepts such as probability and statistical inference.
  • To perform this job successfully, an individual should have knowledge of Internet software, Spreadsheet software, Word Processing software, Graphics software (eg, PowerPoint or Prism), Biliographic software eg, EndNote) and any other applicable software as may be needed by the job from time to time as it changes.
  • Must demonstrate strong experience in relationship building and experience in collaborating with large and strategic accounts.

List #1

Day in the life

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Standing Strong on Ovarian Cancer Day

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Inside ICON

Content type

Blogs

Publish date

05/08/2025

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Standing Strong on Ovarian Cancer Day:    ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen

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Martin Lachs, VP, Oncology Project Management at ICON discusses ICON’s role in advancing ovarian cancer research.

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Nurse and patient
Patient Centricity in Clinical Research

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Industry

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Publish date

05/07/2025

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Patient Centricity in Clinical Research: What it is and Why it Matters In the past, clinical research was designed around the needs of sponsors, researchers, and regulatory bodies. Patients were of

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Discover how patient centricity is reshaping clinical research by placing participants at the heart of study design and execution.

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Navigating Regulatory Landscapes - FDA, EMA, & MHRA

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Navigating Regulatory Landscapes:     Comparing FDA, EMA, & MHRA in Clinical Trials In clinical research, no matter how promising a new therapy may be, it will go nowhere without regulatory appro

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Compare FDA, EMA, and MHRA regulatory frameworks for clinical trials, and why this knowledge matters.

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