Accountable for the planning, coordination, and conduct of trial activities according to ICH-GCP
Assures the seamless conduct of trials within defined timelines in close coordination and communication with the Clinical Trial Leader (CTL)
Collaborate and interact with other core and extended trial team members
Ensure cooperation with external functions (i.e. Clinical Research Organizations, advisors, investigators)
Independently manage correspondence, complex reports, tracking tools and budget overviews
Oversight of all trial related wrap-up activities (i.e. data cleaning)

Requires a university degree and/or comparable professional education with at least 5 years clinical trials experience
Strong communication skills; articulates and aligns business strategy/plan on an ongoing basis, ensuring alignment between words and action
Proficiency with Windows, MS Office (Word, PowerPoint, Excel, Outlook)
Proficiency in written and spoken English and (local language)

Clinical Trial Operations Specialist

Key skills