Role & responsibilities :

Job Description of a CRC includes, but is not limited to, the following:

- Ensure all start up activities are completed as per plan and committed timelines
- Ensure that pre-study documents are collected with highest level of quality, site staff is trained or certified as per study requirements
- Ensure site readiness before SIV which includes Ethics approvals, CTA signatures and other site initiation requirements of the sponsor
- Pre-screening and identification of patients as per protocol and assist PIs in screening patients
- Meeting and exceeding enrolment targets
- Ensuring 100% patient retention and that they complete all visits within visit window and also complete all study visits
- Performing all patient visit activities for the assigned masked/unmasked role
- Ensuring data entry, query resolution, hosting monitoring and other study visits including audits and inspections
- Manage patient safety and ensuring all safety reporting as per protocol/process and regulations

Preferred candidate profile

Having Experience as Clinical Research Coordinator

📌 Clinical Research Coordinator (Odisha)
🏢 PFC Pharma Focus
📍 Odisha