As a Principal Medical Writer, you will join 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 related to the preparation, compilation, and submission of applications to regulatory authorities worldwide.
What you will be doing:
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You are:
- Holding a Bachelor's degree in a life sciences discipline; a Master's degree is preferred.
- Having at least 6 years of medical writing experience within the biopharmaceutical/CRO industry.
- Experienced in regulatory writing, including Clinical Study Reports, IBs, and Protocols.
- Oncology experience is a plus.
- Possessing a proficient understanding of domestic and international regulatory requirements and therapeutic areas across all phases of clinical development.
- Skilled in organizing and communicating clinical information effectively.
- Demonstrating strong communication, organizational, time management, and project management skills.
Our success depends on the quality of our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Besides a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:
At ICON, inclusion & belonging are core to our culture. We are committed to providing an inclusive, accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.