Description

In this role, you will support clinical trials by managing essential documentation, collaborating with teams, and ensuring compliance. Your day-to-day responsibilities will include mentoring colleagues and contributing to process improvements, all while working from home.

Requirements

• •Bachelor’s or higher-level degree in life science or High School Diploma and apprenticeship in life science, medical or pharmaceutical field, or office management
• •At least 2-4 years experience as Clinical Trial Coordinator or in another administrative role in clinical research
• •Knowledge of clinical research regulatory requirements, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• •Fluent in German at C1 level and good command of English
• •Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
• •Effective communication, organizational and planning skills
• •Ability to work independently and prioritize tasks while working on multiple projects
• •Ability to establish and maintain effective working relationships with coworkers, managers and clients

Tasks

• •Assist Clinical Research Associates with updating and maintaining clinical documents
• •Collaborate on the preparation and distribution of clinical documentation and reports
• •Review study files for completeness
• •Coordinate the management of Clinical Trial Supplies and tracking information
• •Manage the tracking of Case Report Forms and clinical data flow
• •Serve as a central contact for project communications and documentation
• •Mentor less experienced Clinical Trial Coordinators and assist with training
• •Act as a subject matter expert for business processes
• •Participate in quality or process improvement initiatives

Tools & Technologies

Benefits