- Review of pre-study file, during study and post study files, vaccutainer/vial labels, log books, completed ICF and CRFs in timely manner
- Ensuring that all staff involved in the study is trained in protocol
- Ensure that all the activities are been done as per protocol ,SOP s and GCP
- Assessing in pharmacy related activities (like Acceptance, labeling, dispensing, reconciliation and storage of IP s)
- Online monitoring and taking print of the temperature record from the software
- Providing study related information to the Ethics Committee, Contracted hospitals and Insurance company
- Preparation of study up- after completion of the study and send it to technical Documentation
- Preparation of Statistical up- and send it to the respective person
- Review clinical report

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📌 Clinical QC professional (Thane)
🏢 Bio Scientific Research Laboratories (BIOSRL)
📍 Thane