Clinical Trials Administrator - Remote

Overview

The Clinical Trials Administrator supports the conduct of clinical trials through various administrative duties, ensuring compliance with standard operating procedures and facilitating project meetings.

In Short

• Carry out administrative duties to support clinical trial conduct.
• Set up and distribute Investigator Site Files according to SOPs.
• Coordinate and attend project meetings, providing high-quality meeting minutes.
• Assist with Trial Master File (TMF) setup and maintenance.
• Maintain contact lists and project team information.
• Provide reports from tracking tools and other ad-hoc reports.
• Work in a dynamic team environment.
• Excellent opportunities for career development in clinical drug development.
• Emphasis on diversity, equity, and inclusion in the workplace.
• Opportunity to work with global colleagues.

Requirements

• Administrative work experience in an international Clinical Research setting.
• Ability to plan, multitask, and work in a dynamic team environment.
• Excellent computer skills, including proficiency in MS Office.

Benefits

• Training and career development opportunities.
• Strong emphasis on personal and professional growth.
• Friendly, supportive working environment.
• Work with colleagues globally, with English as the company language.