Clinical Research Associate

Role & responsibilities

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 process and protocol adherence

Coordinate with investigators, CRO and sponsor teams on trial timelines

Support adverse event reporting and patient safety documentation

Maintain Trial Master File (TMF) documentation and site files

Preferred candidate profile

Basic knowledge of MS Office (Word, Excel, PowerPoint)

Good written and verbal communication skills

Attention to detail and documentation discipline

Willingness to learn and work in a regulated, compliance-driven environment

Willingness to travel for site visits