南京招聘

岗位职责:

Key Accountabilities
1、Participate in or contributes to protocol development (including study design, sample size calculation, randomization, and statistical analysis methodologies), case report form design and data collection
2、Develop and review statistical analysis plan, tables/listings/figures mock-ups, statistical analysis report and statistical section of clinical study report
3、Interact with clients as key contact with regard to statistical issues
4、Work with programming team to complete a project according to the requirements, QC/review the programming deliverables
5、May provide trainings to non-statistical peers with regard to statistical methodologies

Education
MS or PhD in Statistics, Math or Scientific Discipline
Language Skills
Competent in written and oral Chinese and English

Minimum Working Experience
Minimum 2 years Pharmaceutical/Biotech and CRO statistician/biostatistician experience.

任职资格:

Qualifications
1、SAS programming skills with SAS Base, SAS/Macros and SAS/Stat
2、Solid knowledge of experimental design, descriptive and inferential statistics both theoretically as well as applied in clinical trials
3、Ability to use professional concepts to achieve objectives in creative and effective ways
4、Good project management skills
5、Teamwork spirit

康龙化成新药技术股份有限公司成立于2004年，是国际领先的生命科学研发服务企业。经过多年发展，康龙化成打造了全方位的临床前药物研发及临床开发一体化平台，贯穿合成化学与药物化学、生物、药物代谢及药代动力学、药理、药物安全评价、放射标记代谢、工艺研发、GMP生产及制剂研发临床试验及临床样品的分析服务等各个领域，提供包括苗头化合物探索与靶标验证、先导化合物优化、临床前候选药物筛选、临床候选物的确认及临床开发、新药临床研究申请和新药申报等一体化研发服务。康龙化成在中国、美国、英国均有运营实体，全球员工人数15000+，业务遍及全球，服务客户包括世界前20大医药公司在内，已超过1500家。