Senior Medical Writer - 1 year contract
- Any EMEA Location, UK
- Medical Writing
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
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As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
As a Senior Medical Writer you will be supporting a Top-5 pharma company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. While being stably employed with ICON, you will be fully embedded with our client. This is 1 year fixed term contract
- Independently produces clinical and regulatory documents in collaboration with Principal Medical Writers . These documents may include clinical study level documents such as clinical summary documents, briefing books and response documents, PIPs .This includes Phase 1 in patients to Phase 3 across multiple therapeutic areas.
- Thoroughly analyze and critically interpret data to determine the best approach to composing each document, applying lean writing strategies.
- Acts as the primary contact for the study team in relation to the preparation and timelines (incl. planning) of assigned documents.
- Facilitates the review of the documents and ensures that documents are submission-ready and finally approved. When preparing documents you will be directly in contact with QC personnel and publishing specialists who support you in document preparation.
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- Minimum requirement of a bachelor’s degree; Master's degree preferred
- 3-5 years Medical Writing experience or other relevant pharmaceutical experience combined with scientific and regulatory knowledge
- Strong writing skills and the ability to convert scientific data into a clear, scientifically sound, well-structured messages.
- Proficient in independently writing several types of clinical/regulatory documents (mainly clinical summary documents, briefing books and response documents ) including leading creation, coordination of the authoring functions, facilitation of the review of the documents and ensuring that documents are submission-ready and finally approved.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
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