Clinical Trials Associate

• Arrange and track system access for project team members
• Maintain and quality audit current document revisions 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 it to the trial master file
• Track and maintain project-related information, including site medical question and answer logs
• Generate and distribute minutes for project-related meetings, including Sponsor and Internal Management meetings
• Maintain current participating site and personnel information
• Arrange and track project-specific training distribution to the project team
• Perform other assigned duties

• Degree level qualification or equivalent experience
• Minimum of one year of experience in a related role
• Skill sets and proven performance equivalent to the stated requirements
• Excellent written and verbal English
• Fluency in the language of the country of location
• Strong interpersonal skills
• Ability to work independently and as a team member
• Ability to adapt in a fast-paced and rapidly changing environment
• Ability to handle multiple tasks and exercise independent judgment
• Strong attention to detail and focus on quality
• Strong organizational and problem-solving skills
• Excellent MS Office skills, including Outlook, Word, Excel and PowerPoint
• Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations, as applicable

• Equal employment opportunities regardless of protected characteristics
• Diverse and inclusive work environment
• Supportive and collaborative teams
• Accessible leadership
• Employee opportunities to succeed and thrive