Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management, ensuring trials are conducted according to approved protocols and regulatory standards
Job Summary
Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management, ensuring trials are conducted according to approved protocols and regulatory standards.
You will conduct remote or on-site visits to assess compliance, manage documentation, and maintain collaborative relationships with investigational sites while ensuring audit readiness.
This role requires frequent travel, generally 60-80%, with exposure to biological fluids and personal protective equipment usage in office, laboratory, clinical, and home office environments.
Matching Summary
Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management, ensuring trials are conducted according to approved protocols and regulatory standards.
Skills & Requirements
Must-have
clinical monitoring skills
risk-based monitoring approach
ICH-GCP guidelines compliance
protocol and regulatory compliance
data accuracy through SDR and SDV
effective communication with medical personnel
frequent travel 60-80%
Nice-to-have
critical thinking and root cause analysis
problem-solving skills
organizational and time management skills
teamwork and independent work capability
good presentation skills
computer skills including Microsoft Office
attention to detail
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
Minimum 1 year clinical research monitoring experience or PPD Drug Development Fellowship completion