Clinical Trials Assistant, Single Sponsor dedicated, office-based in Kyiv, Ukraine
IQVIA · Kyiv, Ukraine · Global
Clinical Research
–
Not yet analysed
Demand62
Career growth58
Healthcare fit70
Remote potential10
5-year outlook
Entry-level CRO assistant pay is typically modest, with meaningful uplift on progression to CRA, CTM, or sponsor-side roles within 3-5 years. Exact figures vary widely by market and cannot be stated without posting data.
Clinical license
Not required
Applicant reach
broad
Seniority
entry
Employment type
–
Date found
2026-09-28
Intelligence details
Why this is worth applying to
Worth considering for clinicians in Ukraine seeking a low-barrier entry point into the CRO/clinical research industry, especially as a stepping stone to CRA or trial management. The thin posting means you should clarify duties, contract terms, and progression before committing.
Who should apply
IMGs and internationally trained doctors, nurses, pharmacists, and healthcare graduates based in or able to work in Kyiv who want to move into clinical research operations. Also suitable for early-career life-science graduates with strong documentation and English skills.
CV angle
Reframe clinical experience around documentation accuracy, protocol adherence, patient record management, and regulatory compliance rather than direct care. Emphasise any exposure to research, audits, quality checks, data entry systems, and GCP training, plus English and local-language proficiency and MS Office/CTMS familiarity.
Skills to highlight
- Clinical documentation and record accuracy
- ICH-GCP awareness
- Regulatory and protocol compliance
- Data entry and database accuracy
- Trial Master File / document management
- Attention to detail and quality checking
- Stakeholder communication (sites, monitors, sponsor)
- MS Office / CTMS / eTMF tools
Role summary
An entry-level CRO position supporting a single sponsor's clinical trials from an IQVIA office in Kyiv, covering trial documentation, data entry, TMF maintenance, and coordination with study sites and internal teams. It is an administrative research-operations role with no direct patient care.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.