FSP Clinical Research Associate I/ Clinical Research Associate II
Thermo Fisher Scientific · Remote, Israel · Global
Clinical Research
Remote
Not yet analysed
Demand90
Career growth85
Healthcare fit85
Remote potential60
5-year outlook
CRA roles typically see steady salary growth with experience, moving from entry-level to senior CRA or CTL positions. Compensation is competitive, often including bonuses and benefits, but exact figures vary by region and sponsor.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
–
Date found
2026-09-22
Intelligence details
Why this is worth applying to
Yes—this is a strong entry point for clinicians transitioning into clinical research, offering a structured path with a global CRO. Clinical experience is highly valued, and the FSP model provides stability.
Who should apply
Doctors, nurses, pharmacists, and allied health professionals with clinical trial exposure or strong clinical knowledge who want to move into research monitoring. IMGs and healthcare graduates with relevant internships also fit.
CV angle
Highlight direct patient care experience as evidence of understanding clinical protocols, patient safety, and data collection. Emphasize any prior involvement in research, audits, or quality improvement.
Skills to highlight
- ICH-GCP guidelines
- Clinical trial monitoring
- Site management
- Data verification
- Regulatory compliance
- Communication
- Problem-solving
Role summary
A Clinical Research Associate (CRA) at Thermo Fisher Scientific's FSP (Functional Service Provider) model monitors clinical trial sites, ensures protocol compliance, verifies data accuracy, and manages site relationships. This is a non-clinical, research-focused role ideal for healthcare professionals transitioning into the clinical research industry.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.