About this role

Designing, planning, coordinating, and conducting all activities involved in clinical research studies
Acting as primary contact and clinical trial expert for study site personnel
Performing site assessments and qualification visits to support site selection decisions
Developing and managing key study site documentation
Participating in and overseeing CRO delivery of site management activities
Validating product performance claims, supplying data for regulatory submissions
Executing site management activities for sponsored studies in assigned focus areas
Working with local and global study teams to achieve business goals

Bachelor's degree in Science Degree preferably in Health Sciences or engineering (or equivalent combination of education and work experience)
3 years of working experience in Medical Device or Diagnostics industry
2 years of working experience in clinical study of IVD/Medical Device/Drug
Excellent understanding of ICH GCP guidelines in execution of clinical trials
Ability to make sound decisions and analyze and solve problems
Flexibility and adaptability to perform in a fast-paced, matrixed environment

Clinical Site Manager – Systems and Automation

Key skills