Clinical Trials Associate

• Provide administrative and project tracking support to clinical project teams
• Ensure assigned project tasks are performed timely and accurately
• Arrange and track system access for project team members
• Maintain and quality audit documents on project portals
• Assist 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
• Track and maintain project-related information, including site medical question and answer logs

• Excellent written and verbal English
• Fluency in the language of the country of location
• Ability to handle multiple tasks and exercise independent judgment
• Strong attention to detail and focus on quality of work
• Strong organizational and problem-solving skills
• Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
• Degree level qualification or equivalent experience
• Minimum of one year's experience in a related role
• Skill sets and proven performance equivalent to the above

• Diverse and inclusive workplace environment
• Supportive and cohesive teams
• Accessible leadership
• Equal employment opportunities
• Employee experiences focused on respect and inclusion