Sr . CRA ( Medical writer )

Bio Scientific Research Laboratories (BIOSRL)

3 - 5 years

2 - 6 Lacs

thane

Posted:1 week ago| Platform:

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Skills Required

biometrics cro cvs pathology blood collection clinical investigator principal investigator vendor counselling monitoring

Work Mode

Work from Office

Job Type

Full Time

Job Description

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

More Jobs at Bio Scientific Research Laboratories (BIOSRL)

Sr . CRA ( Medical writer )

thane

3.0 - 5.0 yrs

INR 2 - 6 Lacs

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