Remote Clinical Trials Associate (Europe)

Visa Hunt; United States; On-site; USD 46,000 - 70,000; Full time

Job summary

Worldwide Clinical Trials, a global CRO, is seeking a Clinical Trials Associate to support the clinical project team with administrative and tracking tasks for multiple projects. This remote role focuses on document control, site files, and timely updates to master files.

The ideal candidate has strong English, excellent MS Office skills, and the ability to manage multiple tasks with high attention to detail. Prior supporting roles in a regulatory environment are a plus.

Qualifications

• Degree level qualification or equivalent experience with minimum one year in a related role.

Responsibilities

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
• Maintain and quality audit to ensure the most recent revisions of documents are on the project portals
• Assist the project team with the preparation and shipment of clinical trial documentation, including the Investigator Site File
• Maintain version and quality control of project documentation and submit to the trial master file
• Assist with the tracking and maintenance of project-related information, including site medical questions and answer logs

Skills

English fluency

Task management

Attention to detail

Organization

Problem-solving

MS Office

Education

Degree level qualification or equivalent

Tools

MS Office

Job description

Worldwide Clinical Trials, a global CRO, is seeking a Clinical Trials Associate to support the clinical project team with administrative and tracking tasks for multiple projects. This remote role focuses on document control, site files, and timely updates to master files.

The ideal candidate has strong English, excellent MS Office skills, and the ability to manage multiple tasks with high attention to detail. Prior supporting roles in a regulatory environment are a plus.