Overview
Provides administrative and technical support to clinical trial project teams, with a focus on audit readiness, site activation, feasibility, documentation, and study systems.
What you'll do
- Coordinate and complete assigned trial activities according to the task matrix.
- Review department, country, investigator, and trial files and document findings.
- Support site activation, feasibility activities, site selection, and regulatory submissions.
- Maintain clinical trial systems, databases, trackers, study documentation, and team lists.
- Process, transmit, compile, and distribute trial documents, reports, supplies, and communications.
- Analyze study metrics, survey data, and findings and escalate risks or non-compliance.
- Train new personnel and collaborate with project teams, sites, vendors, and internal departments.
What you'll need
- 0–1 year of comparable previous experience.
- High or secondary school diploma or equivalent and relevant academic or vocational qualification.
- Ability to work independently and in a team while managing multiple tasks.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Good English and relevant local-language skills.
- Knowledge of applicable regulations, ICH Good Clinical Practices, and applicable SOPs.
- Strong organization, communication, judgment, decision-making, and risk-management skills.
Nice to have
- Bachelor's degree preferred.
Details
- Remote role in Serbia.
- Standard Monday–Friday schedule.
- Occasional travel or drives to site locations may be required.
Read the full description and apply on the company’s own careers page.
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