Senior Clinical Trials Associate

• Arrange and track system access for project team members, including Project Managers, Lead CRAs, and CRAs
• Maintain and quality audit project portal documents to ensure the most recent revisions are available
• Assist with preparation and shipment of clinical trial documentation, including Investigator Site Files
• Maintain version and quality control of project documentation and submit documents 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
• Provide administrative and project tracking support to clinical project teams
• Ensure assigned project tasks are performed timely and accurately

• Excellent written and verbal English
• Fluency in the language of the country of location
• Strong interpersonal skills
• Strong attention to detail and focus on quality of work
• Strong organizational and problem-solving skills
• Degree level qualification or equivalent experience
• Minimum of two years’ experience in a related role
• Skill sets and proven performance equivalent to the above

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law
• Diverse and inclusive work environment
• Supportive teams and accessible leaders
• Opportunities to collaborate and be creative