Maintaining the source documents CRF s Investigator Site File and other study related documents according to ICH-GCP guideline Completing the eCRF Maintenance of Investigational Product according to the specific temperature Preparing for site qualification visits initiation visits monitoring visits and site close out visits Organizing ethics committee meetings Completing the review forms and submitting all study related documents to EC Coordinating with the local labs central labs Assistance in Safety Reporting within the required timelines Assistance in patient selection and recruitment Assistance in Informed Consent Process Job Type Full-time Qualification Fresher in Science Field Schedule Day shift Job Type Full-time Pay 5 000 00 per month Benefits Adaptable schedule Work Location In person
📌 Clinical Research Co-ordinator (Viluppuram)
🏢 Nameless
📍 Viluppuram
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