Clinical Research Associate II / Senior Clinical Research (CRA) - UK
CTI · United Kingdom · GB
Clinical Research
Remote/Hybrid — check advert
Not yet analysed
Demand82
Career growth78
Healthcare fit72
Remote potential55
5-year outlook
CRA II/Senior CRA roles in the UK typically offer solid compensation with progression into lead CRA, clinical trial management, or clinical operations leadership; exact salary depends on experience, CRO, and therapeutic area.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-07
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Eligible countries
- United Kingdom
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying if you already have 3-5 years of CRA/monitoring experience and want a global CRO with structured development and hybrid work. Clinicians without CRA experience should build monitoring or site coordination experience first.
Who should apply
Experienced CRAs, clinical research nurses, physicians, pharmacists, or life science graduates with 3-5 years of clinical trial monitoring experience, especially those seeking CRO roles in the UK.
CV angle
Frame clinical experience around trial monitoring, site management, source document verification, ICH-GCP compliance, regulatory documentation, investigational product handling, and cross-functional project teamwork; quantify sites monitored, patients/data reviewed, and therapeutic areas.
Skills to highlight
- Clinical trial monitoring
- Source Document Verification (SDV)
- ICH-GCP
- Regulatory compliance
- Investigational product (IP) management
- Site management
- Clinical research
- Project team collaboration
Role summary
A CRA II/Senior CRA at CTI monitors clinical trial sites in the UK, performing source document verification, managing regulatory documents and investigational product, and ensuring ICH-GCP compliance as part of a global project team.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.