Centralized Monitoring Assistant

IQVIA · Sofia, Bulgaria

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Clinical OperationsFull-timeCompany career page

The apply link worked recently (not employer-confirmed).

Role summary

Entry-level administrative role supporting centralized monitoring activities in clinical research. The position involves completing training and performing administrative tasks under supervision to support project execution while maintaining compliance with regulatory standards.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-06). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in life sciences or equivalent education
Up to 6 months relevant experience or equivalent combination of education and training
Knowledge of ICH GCP and applicable regulatory requirements
Proficiency in Microsoft Word, Excel, and PowerPoint
Strong written and verbal English communication skills
Detail-oriented with effective time management abilities
Proficient data entry and phone communication skills

What you'll be doing

Complete role-specific training in accordance with SOPs and regulatory requirements
Execute administrative tasks to support team members including report generation and document preparation
Maintain project systems and study documentation within established timelines
Perform assigned activities as directed by Centralized Monitoring Specialist or Lead

Privacy & handoff

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What RoleLantern checked

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