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Responsible for conduct of Qualification visit, Site Initiation Visit, Monitoring Visit and Closeouts
Would be the first point of contact for Communication with the Investigators and site
personnel’s for the study assigned.
Coordinate the movement of Laboratory samples if applicable.
Ensuring the data entry/CRF filling, following-up visits of subjects as per the protocol.
Prepares follow up letters and reports for the respective visits as per the SOPs and share with
the site and Sponsor as required.
Follow-up with the coordinator for the query resolution.
To collect the collated Ethics Committee documents from CTA for EC submission as defined in
To ensure that the interim safety reports, interim study reports are provided to EC as per the
governed regulatory body.
Preparation of power point presentations for investigator meetings and Site Initiation visits.
Managing the CRC activities, and training them periodically.
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Indian Healthcare BPO
Global Hospital and Pharmaceutical Research Centre
SciEnhns Scientific Solutions Pvt Ltd