About this role

Responsible for designing, planning, coordinating and conducting clinical research studies
Act as primary contact and clinical trial expert for assigned study site personnel
Perform site assessments/site qualification visits in the site selection decision process
May participate in site activation including obtaining necessary approvals
Develop key study site documents and collaborate cross-functionally with R&D
Deliver all data generation/validation and site monitoring activities

Bachelor's degree in a scientific discipline
3 years of experience in a regulated, CRO, diagnostic and or pharmaceutical industry
Experience with clinical trial management and bio-sample management
Experience validating product performance claims and supplying data for Regulatory submissions
Executed Site Management activities for sponsored studies for registrational and/or non-registrational purposes
Worked in local and global study teams, including virtual teams and exhibit diversity and cultural awareness
Built and maintained strong, collaborative relationships with cross-functional team members and stakeholders

Clinical Site Manager

Key skills