As a Senior 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 Senior 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.
The role involves frequent travel, generally 60-80%, with exposure to biological fluids and requires compliance with specific sponsor/client/site requirements.
Matching Summary
As a Senior 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
Risk-based clinical monitoring
ICH-GCP guidelines compliance
Clinical Trial Management System proficiency
Root cause analysis and problem solving
Remote and on-site monitoring
Regulatory documentation management
Nice-to-have
Effective oral and written communication
Strong attention to detail
Team collaboration and independent work
Good presentation skills
Adaptability in diverse scenarios
Customer focus and interpersonal skills
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
Minimum 2 years clinical research monitoring experience