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.
Our mission is to enable our customers to make the world healthier, cleaner and safer through accelerating research and supporting patients in need.
Work is performed in office, laboratory, clinical, and home office environments with frequent travel of 60-80%, including exposure to biological fluids and use of personal protective equipment.
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 compliance
Protocol and regulatory compliance
Remote and on-site monitoring
Clinical trial documentation management
Fluency in Arabic and English
Nice-to-have
Critical thinking and root cause analysis
Good presentation skills
Effective interpersonal skills
Ability to work independently or in a team
Good computer skills including Microsoft Office
Attention to detail
Customer focus and communication skills
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
2 years clinical research monitoring experience or PPD Drug Development Fellowship completion
Valid driver's license where applicable
Experience monitoring observational, RWE, non-interventional trials in GCC and Levant
Fluency in Arabic and good English language skills