As a Clinical Research Coordinator you are the day-to-day engine of the site. You will screen and enrol participants, schedule visits, maintain source documents and essential documents, and act as the main point of contact for participants, monitors and the sponsor.
You will work closely with the Principal Investigator and our operations team on live studies, gaining hands-on exposure across the trial lifecycle.
Responsibilities
Screen and enrol eligible participants per the protocol
Maintain accurate source documents and the investigator site file
Coordinate study visits and required assessments
Support informed consent and ethics committee submissions
Prepare for and support monitoring visits
Requirements
Life-science, pharmacy, nursing or medical graduate
Positive communication and organisational skills
Attention to detail and a quality-first mindset
GCP awareness is a plus (training provided)
Ready to apply for this role
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📌 Clinical Research Coordinator (Gurugram)
🏢 Clins Research
📍 Gurugram
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