- Manage and execute tasks in line with company SOPs and agreed regulatory standards.
- Maintain accurate records, including real-time tracker updates and high-volume email communications.
- Direct support staff activities, ensuring quality and timely delivery of project tasks.
- Procure licenses and permissions, establishing written agreements in collaboration with Legal.
- Research, identify, and perform preliminary assessments for scale source documents.
- Establish and maintain relationships with copyright holders and third-party vendors.
- Oversee the production and quality control of study-specific materials and scale modifications.
- Liaise with clinical science leads and sponsor teams to ensure adherence to study timelines.
Project ManagementMicrosoft Office