Medical Writer
About the role
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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
General Medical Writing (Sr Medical Writer)
- 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.
Narrative Writing (All levels)
- Write patient narratives for serious adverse events and drop-outs due to non-serious adverse events; write the reports of clinical trials and other regulatory documents (including) according to ICON or client-specified formats
- Provide additional writing and editing services (e.g. for publications) as required
- Assist in the production of preclinical summaries, clinical summaries, pharmacokinetic reports, safety summaries, literature reviews, and other documents needed for regulatory submissions
Candidates are expected to
- 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 where applicable.
What you need
- Bachelors degree in a life science/health related sciences, or equivalent
- Medical/Technical writing experience of 3 to 14 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.
Benefits Of Working In ICON
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
Why join us
Other than working with an outstanding team of ambitious people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
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.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
EOE race/colour/religion/sex/sexual orientation/gender identity/disability/vet/national origin
#LI-BIO1
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
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12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
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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
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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
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