Consultant Medical Writer - Regulatory and Clinical Documents
| Dyddiad hysbysebu: | 07 Hydref 2025 |
|---|---|
| Cyflog: | £80.0 i £110.0 yr awr |
| Gwybodaeth ychwanegol am y cyflog: | £80 - 110 p/h Outside IR35 |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 14 Hydref 2025 |
| Lleoliad: | City of London, London, EC2V 6DB |
| Gweithio o bell: | Yn gyfan gwbl o bell |
| Cwmni: | Hays Specialist Recruitment |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | 4731988_1759857526 |
Crynodeb
Your new company
Are you a seasoned Medical Writer with expert experience of writing Clinical and Regulatory documents?
Our client, a global biopharmaceutical powerhouse, is seeking a Consultant Medical Writer to lead strategic and operational excellence across their Oncology portfolio.This is a high-impact, global role offering the chance to influence regulatory strategy at the highest level and join a forward-thinking organisation that values transformation, quality, and scientific integrity.
Remote
OUTSIDE IR35
Your new role
As Director, Medical Writing, you'll be the go-to expert for all medical writing activities within the Oncology Therapeutic Area.
You'll:
Oversee a team of Senior Medical Writers and Managers across global hubs.
Develop and execute TA-specific medical writing roadmaps aligned with R&D priorities.
Oversee and provide input on all documents for clinical development from FIH through Phase 3 and Regulatory submissions including regulatory interactions with agencies (e.g., pre-IND, End of Phase 2, End of Phase 3, Type C meetings).
Be highly organised, proactive, respects metrics-driven timelines and accountability for quality.
Ensure consistency and compliance across the therapeutic area documents (protocols through marketing applications).
Drive regulatory storytelling and key message generation for critical submissions.
Ensure quality, consistency, and compliance across all deliverables.
Manage outsourced writing models and vendor relationships.
What you'll need to succeed
Proven experience in medical writing leadership within oncology or a related TA.
Expert experience of writing documents for clinical development from FIH through Phase 3 and Regulatory submissions including regulatory interactions with agencies (e.g., pre-IND, End of Phase 2, End of Phase 3, Type C meetings).
Deep understanding of global regulatory requirements and submission strategy.
Strong background in clinical development and cross-functional collaboration.
Exceptional communication, negotiation, and strategic thinking skills.
A passion for innovation, including AI-assisted writing and process transformation.
What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and residing in the UK.
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Roberta Atkins on 03330106292