Experienced Clinical Trial Assistant

IQVIA Inc; Riyadh; On-site; SAR 150,000 - 200,000; Full time

Job summary

A leading global provider of clinical research services is seeking an Experienced Clinical Trial Assistant in Riyadh. The role involves supporting clinical documentation, managing project communications, and assisting with trial-related activities to ensure compliance and efficiency. Applicants should have administrative experience, ideally in a clinical research setting, and excellent communication skills.

Qualifications

• 3-4 years of administrative support experience.
• Minimum one year of clinical research experience preferred.
• Basic knowledge of GCP and ICH guidelines.

Responsibilities

• Assist CRAs and RSU teams with updating clinical documents.
• Manage Clinical Trial Supplies and documentation.
• Support CRAs during site visits for monitoring duties.

Skills

Communication

Time Management

Organizational Skills

Microsoft Excel

Microsoft Word

Microsoft PowerPoint

Education

High School Diploma or equivalent

Job description

Experienced Clinical Trial Assistant

Locations

Riyadh, Saudi Arabia

Time Type

Full time

Posted On

Posted Today

Job Requisition ID

R1488020

Job Overview

Perform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure complete and accurate Trial Master File delivery.

Essential Functions

1. Assist CRAs and RSU teams with updating and maintaining clinical documents and systems (e.g., TMF) to track site compliance and performance within project timelines.
2. Handle the preparation, distribution, filing, and archiving of clinical documentation and reports according to SOPs.
3. Review study files periodically for completeness.
4. Assist with the management of Clinical Trial Supplies, CRFs, queries, and clinical data flow.
5. Serve as a central contact for project communications and documentation.
6. Support CRAs during site visits for clinical monitoring duties after training.
7. Collaborate on clinical documentation tasks as needed.

Qualifications

• High School Diploma or equivalent
• 3-4 years of administrative support experience
• Minimum one year of clinical research experience preferred
• Proficiency in Microsoft Word, Excel, PowerPoint
• Strong written and verbal communication skills in English
• Effective time management and organizational skills
• Ability to establish good working relationships
• Basic knowledge of GCP and ICH guidelines
• Understanding of protocol requirements

IQVIA is a leading global provider of clinical research services, healthcare insights, and intelligence. We aim to accelerate the development and commercialization of medical treatments to improve patient outcomes worldwide. We value diverse talent, curiosity, and innovation, and everyone at IQVIA contributes to our mission of improving lives globally. We appreciate your interest in growing your career with us.