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| Job Location | Pune |
| Education | Not Mentioned |
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| Industry | Legal |
| Functional Area | General / Other Software |
| EmploymentType | Full-time |
Statistical Programming 5-12 yrs. (Min 3 years study lead experience) Thorough understanding of clinical trial processes, from data collection to analysis reporting Prior experience and ability to lead and manage programmers in successful and timely completion of all programming related activities (include preparing data and programming specifications) for a study end-to-end In-depth knowledge on latest CDISC SDTM, ADaM , and Define standards along with strong ability to implement all aspects of those standards-Excellent project management skills and ability to lead multiple projects effectively. Excellent oral and written English communication skills Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners Willingness and ability to provide guidance to team members on technical and process questions Should be leading at least 1 -4 studies. Depending on the experience level Kindly share cvs to bhagavathy@recruiseindia.com,
Keyskills :
sassasprogrammingsdtmdatamanagementdatacollectionmanagementskillsprojectmanagementcommunicationskillsprojectadministrationclinicaltrialcvsenglishanalysisclinicaltingkeffectivelymanage