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| Job Location | Hyderabad |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | Pharma / Biotech |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
Experience : 1 to 4 yrs in Clinical Research Associative.Responsible for conduct of Qualification visit, Site Initiation Visit, Monitoring Visit and Closeouts visit.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 site SOPs.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,
Keyskills :
site initiationclinical researchcrccrfctavisitethicsfillingtrainingresearchclinicalcloseoutspowerpointmonitinitiationpreparationcommunicationpresentationsstudy repregulating