Senior Medical Writer

Senior Medical Writer - client dedicated

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

We are currently seeking a Senior Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.

What will you be doing?

Researches, writes, and edits clinical and regulatory documents by applying functional expertise and clinical drug development knowledge. Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents. Exhibits excellent written and oral communication and presentation skills. Demonstrates technical expertise and background in the use of medical writing templates and software (eg, PleaseReview, Documentum-based platforms, etc.).

What do you need to have?

• Manages all aspects of the medical writing function.

• Writes and reviews clinical study reports, protocols, and other clinical/regulatory documents.

• Contributes to clinical protocol development for first-in-human oncology studies.

• Demonstrates technical expertise and background in the use of medical writing templates and software (eg, PleaseReview, Documentum-based platforms, etc.).

• Writes clear and concise documents, including study reports, protocols, investigator brochures, summary documents, and other scientific documents

• Drive the document preparation process, receive and review primary statistical output, draft and distribute documents for review, and incorporate/resolve comments with all reviewers.

• Acts as a lead medical writer on complex programs and numerous individual studies.

• Provides scientific and medical writing consultancy to project teams, as requested.

What do you need to have:

• Advanced degree in a relevant scientific/clinical/regulatory field preferred

• At least 3-5 years of experience in a lead oncology medical writing role in the pharmaceutical/CRO industry. *Note: oncology experience is preferred.

• Experience in regulatory writing - Protocols, CSRs, IBs

• Excellent writing skills.

• Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.

• Knowledge of current requirements and guidelines applicable to submission documents

• Excellent interpersonal and oral communication skills.

• Strong knowledge of MS Word, Excel, PowerPoint, and Outlook

• Ability to prioritize multiple projects

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What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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 or submit a request here

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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