1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Review of CRF Design against Protocol and Sponsor Specifications (SSPs).
· Audit of database against the CRF to ensure compliance to Protocol, Regulatory requirements, In-house SOPs and SSPs.
· Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and Software Development activities and communicate audit observations to the respective department. ...
5 Opening(s)
3.0 Year(s) To 8.0 Year(s)
2.00 LPA TO 10.00 LPA
? Generate safety and efficacy tables, listings and Figures for CT Projects and stand-alone studies .
? Validate programs and outputs of developers
? Review Mock shells and CRF.
? Generate SDTM datasets and AdaM datasets as required with respect to allocation
? Validate CDSIC datasets and programs of developers.
? Communicate with cross functional team and sponsor if required for ...