Clinical Research Associate
ICON · Poland
Clinical Research
Remote
Dentist
Demand72
Career growth70
Healthcare fit82
Remote potential25
5-year outlook
CRA II sits in the mid-tier of CRO compensation with structured progression toward Senior CRA, Lead CRA, or Clinical Trial Manager; pay scales with travel tolerance, therapeutic-area breadth, and sponsor-side moves, though exact figures vary by country and should be checked locally.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-11-05
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Profession fit
- Dentist
- 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
A strong, well-trodden exit for clinicians who want trial oversight without patient care, but the 2-year CRA requirement means it is a lateral move for existing CRAs rather than a true entry ramp for most doctors or nurses.
Who should apply
Clinicians with prior CRA, site coordinator, or clinical trial site experience — especially research nurses, pharmacists with trial exposure, and IMGs with GCP familiarity — who are comfortable with ~40% travel.
CV angle
Reframe clinical experience around trial-adjacent evidence: named studies or audits you supported, GCP training, protocol adherence, adverse event reporting, source-document/data accuracy, site or investigator interactions, and any monitoring, query resolution, or regulatory documentation work; lead with ICH-GCP, data integrity, and site collaboration rather than ward duties.
Skills to highlight
- ICH-GCP compliance
- Site monitoring and initiation/close-out visits
- Protocol compliance and patient safety oversight
- Clinical data review and query resolution
- Clinical study documentation and report preparation
- Investigator and site staff collaboration
- Organizational and travel-based time management
Role summary
A CRO-based CRA II position at ICON responsible for monitoring clinical trial sites — qualification, initiation, routine monitoring and close-out visits — ensuring protocol and GCP compliance, resolving data queries, and supporting study documentation across assigned trials.
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