Clinical Research Associate

Role Overview An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies. Key Responsibilities ■ Support and conduct site visits for study initiation, monitoring and close-out ■ Verify source documents against Case Report Forms (CRFs) for data accuracy ■ Ensure clinical trials are conducted as per GCP, ICH guidelines and study protocol ■ Track patient enrolment, informed consent proce…