Senior Medical Writer
hace 2 semanas
About the Role
We are seeking a highly skilled Senior Medical Writer to join our team at ICON. As a key member of our clinical documentation team, you will be responsible for writing and editing high-quality clinical documents in support of regulatory submissions.
Key Responsibilities
- Develop and implement clinical content strategies for assigned projects
- Author and edit clinical documents, including safety summaries, efficacy summaries, and clinical overviews
- Collaborate with cross-functional teams to ensure consistency and accuracy in clinical documentation
- Maintain current knowledge of regulatory agency medical review guidelines and drug approval requirements
Requirements
- 5-6 years of experience in regulatory medical writing, with 4 years of experience in writing submission documents
- Master's degree in natural sciences or a related field; strong candidates with a Bachelor's degree will also be considered
- Thorough understanding of the overall drug development process and clinical study report development process
Why Work at ICON?
At ICON, we offer a comprehensive and competitive total reward package that includes a wide range of variable pay and recognition programs, as well as best-in-class employee benefits and supportive policies.
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