As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
You will Lead, manage, and coordinate all internal and external writing activities associated with the preparation, compilation, and submission of applications to regulatory authorities globally.
What you will be doing:
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You are:
- A Bachelor's degree in a life science discipline, with Master's degree in life science
discipline preferred.
• At least 6 years of medical writing experience in the biopharmaceutical/CRO industry required.
- Regulatory writing experience - Clinical Study Reports, IBs, Protocols
- Oncology experience would be a plus
• Proficient understanding and knowledge of domestic and international regulatory
requirements required and knowledge of therapeutic areas in all phases of clinical
development desired.
• Proficiency in organizing and communicating clinical information necessary.
• Strong communications, organizational, time management, and project management
skills are required.
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:
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.
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