
Senior Clinical Document Specialist
4 days ago
Our Culture
We believe that our people are our greatest asset, and we strive to create an environment where everyone can thrive. Our 'Own It' culture is driven by four key values: Accountability & Delivery, Collaboration, Partnership, and Integrity. These values guide our actions and decisions, ensuring that we always act with integrity, respect, and transparency.
About the Job
This is a rare, home-based opportunity to join our friendly global Medical Writing team, which sits within ICON's Clinical Research Services group. As a Senior Medical Writer, you will be responsible for producing high-quality documents supporting clinical studies and regulatory submissions. You will work closely with cross-functional teams to develop study protocols, synopses, informed consent forms, and data collection documents. Additionally, you will be responsible for developing scientific communication materials such as abstracts, posters, and manuscripts.
What You'll Need
To excel in this role, you will require 5+ years of experience in Medical Writing, preferably in a pharmaceutical, biotechnology, or CRO environment. A PhD in a medical or biological field is preferred. You should have excellent written and verbal communication skills, as well as strong interpersonal skills. Proven knowledge of ICH/GCP guidelines or other relevant regulations is essential. Good computer literacy and the ability to work effectively in a team are also necessary.
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