Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices
Job Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates.
Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct.
Matching Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
Skills & Requirements
Must-have
on-site and remote monitoring
ensure compliance with GCP
develop monitoring tools
manage project components
accurate and timely documentation
collaborate with cross-functional teams
Nice-to-have
passionate problem solvers
innovating as a team
driven to deliver
inclusive culture
shape the future of healthcare
Key Requirements
Bachelor's degree or equivalent experience
2-4 years of experience in clinical research monitoring