Clinical Research Associate
ICON · Bulgaria
Clinical Research
Remote
Dentist
Demand82
Career growth78
Healthcare fit74
Remote potential15
5-year outlook
CRA compensation generally progresses with monitoring experience, therapeutic-area depth, and moves into clinical operations or study management; exact pay varies by country, CRO, and experience level.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-10-20
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
Worth considering if you already have CRA monitoring experience and want to work within a large CRO. Clinicians without prior CRA experience should treat this as a longer-term transition rather than an immediate entry route.
Who should apply
Experienced CRAs, nurses/doctors/pharmacists with prior clinical trial monitoring or site coordination exposure, and healthcare graduates who have worked in CRO or sponsor clinical operations teams.
CV angle
Frame real clinical experience around trial-adjacent work: protocol adherence, patient safety, data quality, site communication, regulatory documentation, query resolution, and ICH-GCP exposure. Quantify study/site volumes and compliance outcomes where true, without inventing CRA duties.
Skills to highlight
- Clinical trial monitoring
- ICH-GCP
- Site management
- Protocol compliance
- Data integrity and query resolution
- Clinical documentation
- Stakeholder communication with investigators and site staff
- Attention to detail in regulated environments
Role summary
CRO-based clinical trial monitoring role responsible for site qualification, initiation, monitoring and close-out visits, protocol/data compliance, query resolution, and study documentation.
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