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Senior Medical Writer

JR066287

About the role

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

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?

At ICON, we have an incredible opportunity for an expert Medical Writer to join our team in Bangalore office. This is a rare opportunity to join our friendly global Medical Writing team which sits within ICON's Clinical Research Services group. Our remit is to produce high quality documents supporting clinical studies and regulatory submissions.

The Role

  • Write clinical trial reports and other regulatory documents

  • Experience in writing CSRs, Protocols, Investigator Brochures, DSURs, PSURs (safety documents), submission documents

  • Provide additional writing and editing services as required (e.g. for publications)

  • Advise on the content and format requirements for clinical reports and regulatory documents

  • Perform quality control (review) of documents and assess whether specific project related documents comply with regulatory requirements, client requests and ICON SOPs

  • Participate in non-project specific activities, including assistance in maintaining the medical writing work schedule

  • Responsible for the daily management of assigned medical writing projects

  • Liaise with project managers and statisticians to ensure the timely implementation of activities related to the production of reports

  • Keep Medical Writing management informed of project status (e.g. in relation to quality, timelines, progress, and problems)

  • Participate in the training and supervision of new and junior medical writers

  • Represent Medical Writing at internal and external meetings

  • Assist Business Development with the preparation of proposals and cost estimates for medical writing tasks

What you need

  • Bachelor's degree in a life science/health related sciences, or equivalent

  • Medical/Technical writing experience of 6 to 11 years in a clinical research setting

  • Outstanding written and verbal interpersonal skills

  • Ability to work effectively and cooperatively with other team members

  • Understanding of clinical research, the drug development process, and applicable regulatory guidelines

Why join us

Ongoing development is vital to us, and as a Medical Writer, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international and we sincerely care about our people and their success.

List #1

Day in the life

Two medics at ICON clinical research clinic
The Strategic Role of Site Selection and Activation in Clinical Trials

Teaser label

Industry

Content type

Blogs

Publish date

07/07/2025

Summary

Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit

Teaser label

Explore the critical role of site selection and activation in clinical trials.

Read more
3 x Digital padlocks
The Role of Cybersecurity in Clinical Data Management

Teaser label

Industry

Content type

Blogs

Publish date

07/04/2025

Summary

Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio

Teaser label

Learn about the critical role cybersecurity plays in an increasingly digital research environment.

Read more
Stethoscope on paper
Specialisations in Clinical Research: Finding Your Niche

Teaser label

Industry

Content type

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07/03/2025

Summary

Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many

Teaser label

Explore the diverse specialisations in clinical research, from clinical operations to data management, regulatory affairs, and beyond.

Read more
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