Responsibilities: Software Quality Assurance with Review and Approval Experience for SDLC Deliverables. Experience should have earlier in career in SDLC/Software Validation with writing and execution of SDLC deliverables (e.g. MVP testin...
Responsibilities: Provide statistical programming support to generate SDTM and ADaM datasets, tables, listings, and figures for individual studies and ISS/Client to FDA, EMA, and other worldwide regulatory agencies. Participate in the re...
Responsibilities: The ideal candidate will have a strong background in regulatory submissions, project management, and cross-functional collaboration within the life sciences industry. Regulatory Strategy and Submissions. Develop and ex...
Responsibilities: The Associate Clinical Research III will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but is not limited to planning and implementation of clinical studies f...