ClinSol GmbH & Co. KG

Clinical Research

• Organise, coordinate, and monitor clinical trials in accordance with ICH-GCP guidelines and internal SOPs
• Recruit, select, and train investigators and study sites
• Conduct study initiation visits, routine monitoring visits (on-site / remote), and close-out visits at study sites throughout Germany
• Communicate with study sites and maintain written documentation
• Identify on-site issues and escalate them to the study sponsor
• Prepare and submit documentation to ethics committees and competent authorities
• Support correspondence activities
• Monitor schedules and deadlines
• Maintain study data in databases (Microsoft Access, Microsoft Excel)
• Support regulatory submission activities and maintain the Trial Master File (TMF)

Clinical Monitor, Clinical Research Associate, CRA

Video Editor

• Reviewing and editing video footage
• Editing and processing content in accordance with style guides for the relevant target platform
• Color correction
• Audio mixing
• Quality control
• Creating overlays and animations
• Supporting the editing and production of daily video content, particularly in post-production

Clinical Monitor, Clinical Research Associate, CRA

Working Student – Video Editing