The Senior CRA plays a critical role in data integrity, patient safety, and overall quality of clinical trials conducted at investigative sites
Job Summary
The Senior CRA plays a critical role in data integrity, patient safety, and overall quality of clinical trials conducted at investigative sites.
The Senior CRA independently monitors trials either onsite or remotely, ensuring compliance with protocols, ICH-GCP guidelines, ICON and/or customer SOPs, and applicable regulatory requirements.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
The Senior CRA plays a critical role in data integrity, patient safety, and overall quality of clinical trials conducted at investigative sites.
Skills & Requirements
Must-have
ICH-GCP guidelines compliance
FDA regulations knowledge
Site readiness for audits
Independent site monitoring
Neurovascular trial monitoring
Nice-to-have
Mentoring junior staff
Fostering inclusive environment
Problem-solving and risk mitigation
Tailoring communication style
Key Requirements
Bachelor's degree required
3 years of monitoring experience
Medical device monitoring experience
Pharma monitoring experience considered
Neuro or Neurovascular monitoring experience a plus