VISAKHAPATNAM · FULLTIME
Clinical Research Associate
Airvin Skills
Visakhapatnam · hybrid · Posted 1d ago
About a minute. You'll make an account on the way through.
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Section · 01
About this role
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
Sourced from naukri
Section · 02