Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management processes
Job Summary
Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management processes.
You will ensure trials are conducted in accordance with approved protocols, ICH-GCP guidelines, and applicable regulations to guarantee subjects' rights and data reliability.
The role involves frequent travel, effective communication with investigative sites and project teams, and contributing to process improvements and project initiatives.
Matching Summary
Join us as a Clinical Research Associate (Level II) to perform and coordinate all aspects of clinical monitoring and site management processes.
Skills & Requirements
Must-have
Clinical monitoring and site management
Risk-based monitoring approach
Protocol and regulatory compliance
Data accuracy through SDR and SDV
Root cause analysis and problem solving
Microsoft Office proficiency
Frequent travel and site visits
Nice-to-have
Effective communication skills
Critical thinking skills
Team collaboration and independent work
Good presentation skills
Attention to detail
Adaptability and flexibility
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
Minimum 1 year clinical research monitoring experience or PPD Drug Development Fellowship
Valid driver's license where applicable
Working knowledge of ICH GCP and applicable regulations