精鼎医药研究开发（上海）有限公司 招募校园英才


精鼎医药研究开发（上海）有限公司（APEX China Co., Ltd）为成立于2002年4月的外资企业，其集团总部国际精鼎科技股份有限公司（APEX International Clinical ResearchCo., Ltd），成立于1999年3月，系一家于亚太地区从事新药研发服务的临床研究委托机构（Contract Research Organization，简称CRO）。

本公司董事长刘致显先生鉴于亚太地区各医院所之硬、软件环境与专业医师皆具有高度的专业素质及水平，但却缺乏符合ICH-GCP规范要求之临床试验环境，亦无接受ICH-GCP训练的专业医护人员，因此成立了国际精鼎，期望为生技产业尽一份力量。

精鼎医药所提供之临床试验服务内容包含了新药开发策略的拟定与计划、国际临床试验规划执行及整合、临床试验的监测、临床研究数据处理、临床研究统计分析、临床试验总结及统计报告、临床试验稽核服务、新药查验登记事务、国际临床试验相关法规咨询等。新药的研究与开发是一件耗资大、时间长、风险高的事业，平均来说，将一个化合物开发成新药的时间大约需要15年的时间，耗资3亿美元，而由于药物开发必须要和专利保护时间赛跑，因此缩短药物开发时间显得格外的重要，新药能提早一天上市，就能争取上市后多一天的专利保护时间。因此，本公司的专业的临床试验服务，可有效增加新药开发效率及降低成本，达到药厂、病人及精鼎医药三赢的局面。
本集团国际精鼎于亚太地区13个地区成立公司或办事处，分别为上海、北京、台湾、香港、韩国、菲律宾、新加坡、马来西亚、泰国、澳洲、纽西兰、印度及Indonesia，员工总人数达380名，其中本科毕业约为20%，硕士以上学历更达75%，且具有高度的英文基础，加上公司对项目执行的严格监控，业已成为亚太地区规模最大、阵容最坚强、服务项目最完整之专业CRO公司，并已在业界建立高质量的专业形象以及良好的口碑。

HOT 强力征求~~~~~~
临床统计分析师 Statistician
1.        生物统计、数理统计、数学、流行病学、医药卫生或医学系相关之硕士以上学历。
2.        熟悉SAS统计软件及相关程序者。
3.        工作地点：上海市浦东新区。
公司提供：A. 统计专业训练及英文训练课程，并提供良好福利与工作环境。
B. 多样化的职涯发展计划。

校园征才宣讲会~~~~~~
地点：铁生馆二楼宣讲厅
时间：11月5日

本公司亦有其它职缺可供您参考，竭诚欢迎您前来阅览我们的网站：www.apex-cro.com/careers.htm
您亦可投递您的履历至hr1@cn.apex-cro.com          或电洽　+86-21-61609090  分机 1301, 1302
˙        APEX, We Are Asia!
APEX International (www.apex-cro.com), the pioneer CRO based in Asia Pacific,
offers full range services in clinical research from Phase I to IV. Establishe
d in 1999,  APEX currently has operations in 13 locations including Taiwan, Ko
rea, Indonesia, Mainland (Shanghai and Beijing), Hong Kong, Singapore, Malaysi
a, Thailand, India, Australia and Philippines with a total of over 350 employe
es.  Being the leading CRO in Asia Pacific, we continue to expand into major c
ities in China and other Asian countries.  At APEX, you can find your direct l
ink to the essence of clinical knowledge in Asia Pacific.
APEX’s dedicated team of well trained clinical research professionals in the
areas of Feasibility Assessments, Global Project Management, Regulatory Consul
tation, Clinical Monitoring, Medical Monitoring, Data Management, Statistical
Analysis, and Medical Writings. Working for clients worldwide, APEX applies it
s expertise in clinical research and offers the best possible solutions and va
luable insights into the clinical and commercial potential of new products.
Our persistence in developing customized strategy and approach is one of our
greatest strengths. Our knowledgeable staffs in all clinical functions are ded
icated to exceeding expectations by offering unsurpassed service and quality.
We strive to be the best value in the marketplace.  At APEX, we value the pers
onal development of our staff and provide various training programs to elevate
their competence.  We look forward to having you join us. 

l        APEX’s Experience and Strength
APEX, located in the heart of East Asia, has established its foothold in condu
cting a large number of trials that comprise nearly all-therapeutic areas.
APEX’s strength:
1.        Wide geographic settings in 13 locations in Asia including Taiwan, Korea, C
hina (Beijing and Shanghai), Hong Kong, Singapore, Malaysia, Thailand, Indones
ia, Philippines, India and Australia.
2.        Experienced local staffs provide updated epidemic information, potential si
te/PI list and regulatory information.
3.        Full range services in clinical research including feasibility assessments,
regulatory consultation, medical writing, clinical monitoring, medical monito
ring, clinical data management, statistical analysis and site management.
4.        Excellent relationship with local regulatory authorities and investigators.

5.        Successful audit records, internationally proven quality.
6.        Wide therapeutic experiences from phases I to IV trials.
7.        Rigorous patient recruitment plan to insure fast patient recruitment.
8.        Direct clients to success by customized and flexible solutions.
Data Management and Statistics Services
Quality is Our Priority – Speed without Compromise

APEX’s fast growing Clinical Data Management and Statistical Analysis Departm
ent (CDMSA) has professional staff with internal clinical project experiences
reside in Taipei and Shanghai offices. The central management in Taiwan provid
es a series of SOP and job trainings to educate our staff in both locations wi
th the same standards, knowledge and skills to deliver high quality work withi
n the study timelines.  The CDMSA collaborates with the Quality Assurance Depa
rtment to validate and monitor all procedures and documents to meet with ICH-G
CP standards.  CDMSA has successfully established its’ credibility and relati
onship with clients thought the project services.


OUR STRENGTH
l        Elite recruiting program
l        Solid professional trainings
l        Regulatory compliant
l        Update-to-date computer technology
l        Full scale of internal SOPs
l        Fully validated processes
l        Adopting industry standards
l        Commitment to customer satisfaction
l        Flexible resource allocation
l        Project management skills
l        Supportive team spirit 

Example:
Successfully adopted the Electronic Data Capture (EDC) system deliver the data
management tasks and maintained the data quality met the requirements.  Succe
ssfully completed the statistical analysis in a reduced timeline.