具体要求：Qualifications 入职资格 - Bachelor degree (master preferred) in Statistics, Biological Sciences, IT, or related field with 3+ years of experiences in pharmaceutical industry - Strong skills in project management requiring little supervision - High competence in SAS programming and Macro development in a clinical data environment (expertise in oncology trials is highly preferred) - Effective communication and collaboration skills in cross-functional team settings - Good knowledge of CDISC data structure requirements - Ability to effectively organize and manage multiple assignments with challenging timelines, from project start-up through BLA/NDA submission - Good knowledge of global regulatory requirements concerning electronic submission standards - Ability to mentor junior staff in programming techniques, project management and communication
