KEMIO Consulting
Clinical Data Manager - RWE - UK Remote
Get notified of more jobs like this · No spam, ever
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Clinical Data Manager – Clinical Trials / Real-World Evidence
Location: UK / Remote
Permanent
KEMIO is looking for an experienced Clinical Data Manager to join a growing Healthcare and Data Analytics Life Sciences organisation delivering observational clinical studies and real-world evidence programmes, with a particular focus on oncology and rare disease.
This is a hands-on role where you'll take ownership of clinical data management activities across Phase II–IV studies, working closely with Clinical Operations, Biometrics, Data Science and Sponsor teams.
What you'll be doing
- Develop and maintain Data Management Plans (DMPs) and data validation specifications
- Support eCRF/EDC design and clinical database development
- Lead data review, cleaning, validation and site query management
- Manage clinical coding including MedDRA and WHO Drug
- Support adverse event/SAE reconciliation and safety data requirements
- Work with multiple data sources including eCOA/ePRO, laboratory, biomarker, EHR, omics and wearable data
- Coordinate data transfers and integrations
- Manage activities through to Database Lock
- Produce data management metrics and KPIs
- Work closely with internal teams and external Sponsors to ensure high-quality, compliant data delivery
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
What we're looking for
You'll have 5+ years' clinical data management experience, ideally gained within pharma, biotech, CRO or a clinical research environment.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
You'll bring strong experience across:
- Phase II–IV clinical studies
- Clinical data review, cleaning and validation
- EDC/eCRF design and edit checks
- Site query management
- MedDRA and WHO Drug coding
- Safety data and SAE reconciliation
- Taking clinical databases through to database lock
- Working within ICH-GCP and relevant regulatory requirements
Experience within oncology and/or rare disease would be particularly valuable. We're looking for someone who can work independently, take ownership of their studies and communicate confidently with both internal teams and Sponsor stakeholders.
Interested in finding out more? Apply via LinkedIn or contact KEMIO Consulting for a confidential conversation.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Location