Job Summary
The Clinical Research Associate plays a crucial role in overseeing clinical trials, ensuring compliance with regulatory standards, and engaging with study staff and investigators. This position requires conducting various phases of research studies effectively and upholding the principles outlined by ICH and GCP.
Responsibilities
- Independently carry out pre-study activities, site initiation visits, and monitoring tasks.
- Provide training to investigators and study personnel during site initiation visits.
- Ensure adherence to ICH/GCP standards throughout the clinical research process.
Qualifications
- Bachelor’s degree in life sciences or a nursing degree.
- At least three years of relevant experience in clinical research.
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