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 ...
2 Opening(s)
3.0 Year(s) To 9.0 Year(s)
2.00 LPA TO 7.00 LPA
Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for BA/BE, Dermatology and In-Vitro studies.
» Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
» Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
» Responsible for ...