Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
Job Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms.
Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Matching Summary
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms.
Skills & Requirements
Must-have
On-site and remote monitoring
Ensure compliance with GCP
Develop monitoring plans
Accurate documentation of findings
Collaborate with cross-functional teams
Nice-to-have
Passionate problem solvers
Innovating as a team
Agile and driven to accelerate delivery
Authentically be yourself
Diversity of thoughts, backgrounds, cultures, and perspectives
Key Requirements
Bachelor's degree or equivalent experience
2-4 years of experience in clinical research monitoring