Remote Clinical Trials Admin & Documentation Specialist

Worldwide; England; Hybrid; GBP 28,000 - 38,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Trials Associate to support the project team across UK and Serbia with remote work. You will handle document control, site file preparation, and QA tracking while ensuring quality and timely delivery.

Applicants should have a degree or equivalent experience and at least one year in a related role, with strong English communication and proficiency in MS Office. This is a full-time remote role offering international opportunities.

Qualifications

• Degree or equivalent with 1+ year in a related role.
• Strong English written and verbal communication.
• Excellent attention to detail and organizational skills.

Responsibilities

• Arrange and track system access for project team.
• Maintain & quality audit latest revisions of documents on project portals.
• Assist with preparation and shipment of site files.
• Maintain version control of project documentation and submit to trial master file.
• Assist with tracking site medical QA log.

Skills

English fluency

Attention to detail

Organizational skills

Problem solving

Education

Bachelor's degree or equivalent

Tools

MS Office

Job description

Worldwide Clinical Trials is seeking a Clinical Trials Associate to support the project team across UK and Serbia with remote work. You will handle document control, site file preparation, and QA tracking while ensuring quality and timely delivery.

Applicants should have a degree or equivalent experience and at least one year in a related role, with strong English communication and proficiency in MS Office. This is a full-time remote role offering international opportunities.