Senior Clinical Trial Manager (Sr. CTM) - Internal Medicine

About the role

PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams.

What you'll do

• Manages all clinical and start-up activities, operational and quality aspects of allocated studies, of moderate to high complexity, in compliance with ICH GCP
• Acts as the primary point of contact for study start-up activities and site activation across the assigned region and/or globally
• Develops start-up and clinical tools (e.g. Essential Document Checklist, Monitoring Plan
• Contributes to the development of the Master Action Plan (MAP) for providing clinical related documents
• Ensures timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central)

What you need

• 5–9 yrs of experience
• Clinical research
• Regulatory affairs
• Communication
• Any graduate