1. Act as primary local company contact for assigned sites for specific trials.
2. Responsible for executing activities within site selection, site initiation and start-up, site monitoring, site management and site/study close-out according to internal SOPs and policies.
3. Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.
4. Ensures accuracy, validity and completeness of data collected at trial sites.
5. Maintains complete, accurate and timely data and essential documents in systems utilized for trial management
6. Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team.
7. Establishes and maintains good working relationships with internal and external stakeholders, in particular investigators, trial coordinators and other site staff.
Qualifications：
1. A minimum of a BA/BS degree is required. A degree in a health or science related field is preferred.
2. Good academic record and internship experience is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
3. Strong IT skills in appropriate software and company systems.
4. Willingness to travel with occasional overnight stay away from home.
5. Proficient in speaking and writing the country language and English, already passed CET-6 test.
6. Good written and oral communication skills.
2、Statistical Programmer Analyst
Objective of Position
Statistical Programmer Analyst is accountable for development, verification, and documentation of SAS code on the assigned clinical project. This role is that of a SAS programmer who is capable of supporting programming requests of low to medium complexity in support of clinical trial reporting and submissions, with guidance.
Main Accountabilities
· Designs and develops statistical programs for the assigned project
· Performs quality control in support of clinical R&D analysis and reporting
· Assists in the review and input into project requirements
· Maintains documentation as appropriate
· Completes programming tasks of low to medium complexity with high quality and timeliness of deliverables
Knowledge
· This role requires an in-depth knowledge of SAS programming
· This role requires a working knowledge of departmental processes and a basic knowledge of clinical research concepts. This role requires a basic awareness of applicable regulations.
Qualifications
· Bachelor’s degree or higher in statistics, mathematics, epidemiology, public health, computer science or other scientific field (or equivalent theoretical/technical depth) is required
· Pharmaceutical industry experience in clinical trial area is a plus
· Experience in a pharmaceutical/clinical trial environment is preferred
· Knowledge of programming language(s) and data structures
· Demonstrated written and verbal communications skill is required
· Experience working with programmers in a team environment is preferred
Minimum Technical Knowledge and Skills
· Expert knowledge of SAS programming. Knowledge of other statistical software (e.g., S-Plus, R, PASS) is a plus
· Good communication skills in written and oral English
【公司介绍】
Janssen China Research and Development Center
We are dedicated to leading the industry inbreak-through innovation.
At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. We focus our efforts and resources on diseases where the unmet need is great, our internal capabilities strongest, and the external science we can partner with compelling. Our goal is to use the best internal and external science to transform how diseases are treated, cured,prevented and intercepted.
Our China R&D Center is one of four hubs for Janssen’s global R&D organization and comprises end-to-end capabilities spanning drug discovery, development and delivery.
· Clinical Development – Based in Beijing and Shanghai, our development work extends to 304 sites, including 111 hospitals with 73 products and compounds in development, including 21 new products or line extensions.
· Discovery Center – Our Shanghai discovery center runs research programs on small and large molecule drug discovery,target validation, and biomarker identification, evaluation and validation, as well as phase 0 clinical trials for hepatitis B,lung cancer, and hematologic malignancies.
· Lung Cancer Center – A cross-sector center of excellence that will transform one of China’s most prevalent forms of cancer into a preventable and curable disease.
· Asia Pacific Innovation Center – One of four J&J Innovation Centers established globally to extend our network and identify early stage collaboration with scientists, entrepreneurs and innovators.
We are dedicated to leading the industry in break-through innovation in China, for China and around the world.
We are Janssen. We collaborate with the world for the health of everyone in it. 作者: zhushou 时间: 2017-10-13 10:50
We collaborate with the world for the health of everyone in it. 作者: zhushou 时间: 2017-10-16 10:44
RE: 强生-杨森中国研发中心 2018校园招聘宣讲会 [修改]
--
作者: zhushou 时间: 2017-10-18 15:41
RE: 强生-杨森中国研发中心 2018校园招聘宣讲会 [作者: zhushou 时间: 2017-10-23 12:47
2018校园招聘宣讲会作者: zhushou 时间: 2017-10-25 14:04
RE: 强生-杨森中国研发中心 2018校园招聘宣讲会作者: zhushou 时间: 2017-10-30 19:16
RE: 强生-杨森中国研发中心 2018校园招聘宣讲会 [修改]作者: zhushou 时间: 2017-11-2 14:03
mplete and accurate at any time point during all trial phases作者: zhushou 时间: 2017-11-6 20:00
2018校园招聘宣讲会作者: zhushou 时间: 2017-11-10 17:54
will transform one of China’s most pr
