- You'll have the opportunity to contribute to releasing groundbreaking therapies for critically ill patients.
- Be inspired by the collective expertise and shared commitment to transforming cancer treatment.
- Work in a dynamic setting that celebrates diversity, experiences, and collaborative efforts.
- Excellent opportunities for professional growth and development alongside experienced professionals and cutting-edge projects.
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Bob W UK London, United KingdomYour keen eye for detail will be crucial as you conduct housekeeping quality audits to maintain our exceptionally high cleaning standards and manage our partnerships with suppliers. Bob's apartments cater to the 21st-century traveller who wants it all: the consistent quality of a ...
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Lead Technical Operator
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Found in: Ziprecruiter UK C2 - 1 day ago
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Regulatory Medical Writing Operations Lead - United Kingdom - Skills Alliance
Description
**Exclusive 6 Month Contract (20 hours) – Medical Writing Operations Lead – Remote, UK **
Are you an experienced Medical Writing Operations Lead passionate about pioneering therapies in the biotech industry? Join our innovative client, a pioneer in developing revolutionary CAR-T cell therapies for cancer treatment
Why here?
As a Medical Writing Operations Lead, you will be primarily responsible for all aspects related to document quality review, including data verification, editorial oversight, adherence to company style and regulatory standards, as well as submission ready formatting for routine and non-routine clinical and non-clinical regulatory documents.
Key Responsibilities:
• Provide editorial support and guidance during authoring of regulatory documents, ensuring adherence to company style and industry standards, as well as clarity, consistency, and proper usage of language and grammar.
• Support document authors with submission ready formatting for Word and PDF regulatory documents according to company guidelines and industry standards using company tools and templates, in collaboration with Regulatory Operations.
A bit of what you'll need:
• Quality review and editorial oversight of regulatory documents, and/or a related field in the pharmaceutical or biotechnology industry
• Working with electronic document management systems (EDMS) in a regulatory environment
• Successfully interacting with cross functional team members
If you're interested and would like to find out more, reach out on LinkedIn or send your CV to