Clinical Trial Coordinator - FSP - UK
Thermo Fisher Scientific · Remote, United Kingdom · Global
Clinical Research
Remote
Not yet analysed
Demand75
Career growth68
Healthcare fit78
Remote potential40
5-year outlook
Clinical trial coordination experience remains useful for progression into CRA, trial management, and clinical operations roles. UK salary progression will depend on GCP experience, therapeutic area exposure, and whether the role sits with a CRO, sponsor, or site.
Clinical license
Not required
Applicant reach
moderate
Seniority
junior
Employment type
–
Date found
2026-10-21
Intelligence details
Flexible work details
- Eligible countries
- United Kingdom
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering for clinicians who want to move into clinical research operations and are comfortable with a coordinator-level CRO/FSP role. Because the description is missing, verify duties, location, remote expectations, and progression before applying.
Who should apply
Nurses, pharmacists, doctors, allied health professionals, IMGs, and healthcare graduates with an interest in clinical trials, research delivery, GCP, and site coordination. Particularly relevant for those seeking a first structured move from clinical practice into clinical research.
CV angle
Frame real clinical experience around protocol adherence, patient communication, accurate documentation, multidisciplinary coordination, data quality, and regulatory awareness. Highlight any audit, research, consent, adverse event reporting, or study-related exposure without overstating involvement.
Skills to highlight
- Clinical trial coordination
- ICH-GCP awareness
- Patient recruitment and consent support
- Data collection and accuracy
- Regulatory documentation
- Site and stakeholder coordination
- Clinical communication
- Attention to detail
Role summary
Coordinates clinical trial activities for a CRO/FSP model in the UK, supporting site operations, patient recruitment, data collection, regulatory documentation, and trial compliance. The posting lacks a detailed description, so exact duties and requirements should be confirmed.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.