This role offers the opportunity to perform and coordinate all aspects of clinical monitoring and site management for top pharmaceutical companies across 100+ countries
Job Summary
This role offers the opportunity to perform and coordinate all aspects of clinical monitoring and site management for top pharmaceutical companies across 100+ countries.
The Senior Clinical Research Associate will conduct remote or on-site visits to assess protocol compliance, manage documentation, and ensure audit readiness.
Candidates must possess strong critical thinking skills to apply root cause analysis and implement corrective actions to decrease site risks.
Matching Summary
This role offers the opportunity to perform and coordinate all aspects of clinical monitoring and site management for top pharmaceutical companies across 100+ countries.
Skills & Requirements
Must-have
3+ years clinical research monitor experience
Bachelor's degree in life science or nursing
Valid driver's license required
60-80% travel frequency
ICH-GCP and FDA guidelines knowledge
Risk-based monitoring approach application
Nice-to-have
Mentoring and training junior team members
Critical thinking and root cause analysis skills
Effective communication with medical personnel
Process improvement identification abilities
Flexible adaptation to changing scenarios
Key Requirements
Bachelor's degree in life science or nursing certification