As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation
Job Summary
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Frequent travel is required, generally 60-80%, including site visits and potential extended overnight stays.
Matching Summary
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
Skills & Requirements
Must-have
Clinical monitoring skills
Risk-based monitoring approach
ICH-GCP guidelines compliance
Protocol and regulatory compliance
Data accuracy review
Travel up to 80%
Microsoft Office proficiency
Nice-to-have
Critical thinking and problem solving
Effective communication skills
Organizational and time management
Interpersonal skills
Presentation skills
Flexibility and adaptability
Team and independent work capability
Key Requirements
Bachelor's degree in life sciences or equivalent
Registered Nursing certification or equivalent
Minimum 1 year clinical research monitoring experience