- Preparation of Protocol, study specific informed consent form and other regulatory documents
- Preparation of Clinical Study Report after completion of study
- Preparation and review of clinical SOPs
- Raise change control documentation for clinical SOP, Instrument and equipment
- Performing screening related activity like registration, biometric verification, demographic examination, alcohol consumption test, drug of abuse test

6) Assist the principal investigator in conduction of protocol meeting
- Distribution of ICF for volunteers and group counselling of subjects
- Assist the physician/ Principal investigator/ Clinical investigator in presentation of informed consent form
- Preparation of labels for sample collection and sample storage
- Conducting and monitoring dispensing and dosing activity
- Performing sample processing,



sample segregation and transfer activity
- Monitoring clinical activities like blood collection, sample processing, meals and restriction activities
- Preparation, reviewing and compilation of study documents (TMF, CRF, ICF etc)
- Recording the subject check in and check out details
- Coordinate with clinical vendor like canteens, pathology lab, hospital, ambulance services, insurance company for study intimation

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📌 Sr . CRA (Thane)
🏢 Bio Scientific Research Laboratories (BIOSRL)
📍 Thane