Global Senior Project Specialist (Sponsor Dedicated) Germany

Overview

Global Senior Project Specialist for a sponsor-dedicated single-sponsor partnership in Germany, supporting clinical trial operations and study documentation.

What you'll do

• Set up, maintain, and close out project files and study information across multiple systems.
• Prepare and distribute meeting minutes and action items for internal and external meetings.
• Follow up on action items through closure with team members.
• Maintain timely communication among team members and site staff.
• Keep Project Leadership and CRAs updated on site and study status.
• Support quality assurance activities, including audit/internal review preparation and issue resolution follow-through.

What you'll need

• Associate’s degree (or equivalent) in a relevant life sciences/medical/health field.
• Knowledge of Good Clinical Practice (GCP)/ICH guidelines and applicable regulatory requirements.
• Previous experience as a Project Specialist within a CRO/pharma company.
• Strong organizational and time-management skills; ability to work independently.
• High proficiency with full MS Office applications.
• Strong written and spoken English communication and presentation/interpersonal skills.

Details

• Location indicated as DEU-Remote.