Remote Clinical Trials Associate – Global CRO

Worldwide; United Kingdom; Remote; GBP 30,000 - 42,000; Full time

Job summary

Worldwide Clinical Trials seeks a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are completed accurately and on time in a remote setup.

You will organize access, manage site documentation, and assist with trial-related shipments, maintaining quality control and proper trial master file standards. Strong English skills and MS Office proficiency are essential.

Qualifications

• Degree level qualification or equivalent experience.
• Minimum of one year’s experience in a related role.
• Excellent written and verbal English.
• Strong organizational and problem-solving skills.

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 project portals.
• Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File.
• Maintain version and quality control of project documentation and submit to trial master file.
• Assist with tracking and maintenance of project related information, including site medical question and answer log.

Skills

Attention to detail

Organizational skills

Problem solving

MS Office

Education

Bachelor's degree or equivalent experience

Tools

MS Office

Job description

Worldwide Clinical Trials seeks a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are completed accurately and on time in a remote setup.

You will organize access, manage site documentation, and assist with trial-related shipments, maintaining quality control and proper trial master file standards. Strong English skills and MS Office proficiency are essential.