Job Summary

Provide project and study support to clinical teams by performing centralized monitoring, administrative tasks, data review, and system updates. Ensure all work aligns with SOPs, ICH-GCP, regulatory requirements, and project timelines.

Key Responsibilities

Complete required role training and follow all SOPs and quality standards.

Provide administrative support (run reports, maintain trackers, prepare status updates, follow up on outstanding items).

Update and maintain study systems and support compliance with project timelines.

Assist in preparing i-Site Packs and other study documents.

Perform centralized monitoring activities and assess site/data quality.

Monitor site performance metrics and follow up on missing data, queries, SDV backlog, and visit schedules.

Identify site-level risks and recommend/track corrective actions.

Conduct Subject Level Data Review (SLDR) and escalate issues as needed.

Perform study-specific analytics and support trend analysis.

Handle access management tasks and coordinate with vendors where required.

Act as backup for Centralized Monitors/Senior Centralized Monitors.

Support technical tools (Excel formulas, macros, tool design) as needed.

Maintain effective communication with sites, CRAs, and internal teams.

Qualifications

Bachelor’s/Postgraduate degree in Life Sciences or related field.

At least 1 year in clinical research or centralized monitoring preferred.

Fluent in Dutch

Proficient with MS Office, especially Excel.

Strong communication, organization, and problem-solving skills.

High attention to detail, accuracy, and data quality.

Ability to work effectively with cross-functional teams and external sites.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.