Responsibilities
- Development and documentation of programs used in the production of computer generated outputs for clinical study reports, registration and submission documents, publication requirements plus any other document used to present clinical trials data
- Communicate with statistician and medical manager to fully understand analysis requirements for assigned clinical projects
- Perform all SAS programming tasks with high quality in the agreed timeline, and work closely with data management to assure data quality
- Participate in review of protocol, statistical analysis plan (SAP), data management plan (DMP) and case report form (CRF)
- Preparation of electronic submission of clinical data

Education/Qualifications
- BSc, MSc or equivalent experience in information technology, mathematics, statistics or medical documentation
- In-depth knowledge of Base SAS, SAS/STAT, SAS Graph, SAS SQL and SAS Macro Language. SAS Certification is preferred, not required
- Knowledge of relevant internal and external standards and guidance for clinical development (CDISC, EMEA/FDA, ICH-GCP etc.)
- Effective communication skills and ability to establish and maintain effective working relationships with study team members
- Ability to work under pressure and manage multiple projects simultaneously
- Solid analytical and problem solving skills paired with strong attention to detail
- Experience in CDISC, aCRF and XML is preferred

其他信息

行业要求：全部行业
所属部门：临床开发与注册部