Medical Writer
| Dyddiad hysbysebu: | 16 Medi 2025 |
|---|---|
| Cyflog: | £30,000 i £45,000 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | + benefits |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 23 Medi 2025 |
| Lleoliad: | City of London, London, EC2V 6DB |
| Gweithio o bell: | Hybrid - gweithio o bell hyd at 3 ddiwrnod yr wythnos |
| Cwmni: | Hays Specialist Recruitment |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | 4725029_1758042420 |
Crynodeb
Your new company
Are you a detail-driven communicator with a passion for science and clinical research? We're partnering with a leading global biopharmaceutical company-renowned for its innovation in rare disease therapies-to find a Medical Writer to join their Clinical Development team.This is a fantastic opportunity for someone looking to grow their career in medical writing within a collaborative, science-led environment that values precision, clarity, and impact.
Your new role
As a Medical Writer, you'll play a key role in the development and delivery of high-quality clinical documentation that supports regulatory submissions and scientific publications. You'll work cross-functionally with clinical teams, statisticians, and regulatory experts to ensure documents are accurate, compliant, and aligned with strategic goals.
Key Responsibilities:
Draft and edit clinical study documents including protocols, amendments, informed consent forms, and study reports
Contribute to safety and efficacy documentation such as Investigator's Brochures and periodic safety reports (PBRERs, DSURs)
Manage timelines, meetings, and review cycles for document development
Provide peer review and editing support across regulatory documentation
Support the development of templates and best practices within the medical writing function
Collaborate effectively across clinical, regulatory, and safety teams
What you'll need to succeed
Bachelor's degree or higher (scientific discipline preferred)
Certifications such as AMWA or DIA are highly regarded.
Experience in medical writing within pharma or biotech
Familiarity with clinical trial documentation, protocol design, and regulatory standards
Strong grasp of biostatistics, clinical data interpretation, and medical terminology
Proficiency in Microsoft Office Suite and document management systems (e.g., Veeva, SharePoint)
Exceptional written and verbal communication
Strong project management and organisational skills
Ability to work independently and manage multiple priorities
Detail-oriented with a proactive mindset
What you'll get in return
Work with a pioneering biotech company making a real difference in patient lives.
Be part of a high-performing, supportive team with clear career development pathways.
Hybrid working model with flexibility and autonomy
Competitive salary and benefits package
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