About this role

Own, and are accountable for, the strategic planning, management and performance of assigned clinical trials
Develop and initiate recruitment and retention strategies
Identify successful site mapping, and set up site engagement plans
Manage local study performance and ensure compliance with timelines
Collaborate with Vendor Functional Line Managers, plan and participate in engagement activities
Maintain data quality, patient safety, and compliance with study metrics

University degree in medicine, pharmacy, biology, biochemistry or related natural science
Experience in clinical research is mandatory
Preferably have experience in project management and time as field monitor or site-coordinator
Solid knowledge of clinical development process and relevant therapeutic/disease area(s)
GCP certificate
Strong skills in project management
Data analytic skills and use of digital tools, platforms and systems
Problem-solving and risk-management skills in a clinical study environment
Change management skills
Interpersonal skills with ability to create and foster trustful relationships with several internal and external stakeholders
Fluent in German and English

Clinical Operations Study Country Lead

Key skills