Lianne Ebbing

• Conducted independent research to validate efficacy of solutions, assimilate results and prepare written technical reports.
• Advanced interpersonal, collaboration and time management skills
• Mentor to junior level CRAs and served as a resource for new employees
• Served as observational and performance visit leader
• Facilitated audits and audit resolutions
• Ensured all required training is completed and documented
• Updated applicable tracking systems
• Ability to establish and maintain effective working relationships with investigative site staff
• Verified Serious Adverse Event (SAE) reporting according to trial specifications and ICH-GCP guidelines
• Assessed IP accountability, dispensation, and compliance at the investigative sites
• Performed essential document site file reconciliation
• Ability to focus on detail for extended periods of time; high attention to accuracy
• Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
• Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
• Directed, guided and delegated tasks to teams and developed project schedules, resource requirements and timelines to maintain productivity on goals and objectives.
• Advanced knowledge of applicable policies and procedures, SOPs, work instructions and other guidance documents
• Worked closely with other clinical team members to facilitate timely resolution of trial and/or clinical issues
• Achieved project objectives by troubleshooting experiments and testing practical and creative solutions.
• Provided regular site status information to team members, trial management, and updates trial management tools
• Reviewed and verified accuracy of clinical trial data collected, either onsite or remotely
• Assessed the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and close clinical trials at investigative sites

• Assisted with special events and programs.
• Used strong interpersonal communication skills to convey information to others.
• Maintained clean, neat, and operational facilities to serve program needs.

Unblinded CRA for the Netherlands, Belgium, Germany and the United Kingdom.