上海招聘

GENERAL DESCRIPTION AND RESPONSIBILITIES

o Review CRF
o Develop mock-up TFLs
o Develop analysis data set specification
o Review all tables, figures and listings
o Analyse and interpret data for clinical trials
o Compiles reports, charts, and tables based on established statistical methods
o Perform meta-analyses by pooling data from several studies
o Update knowledge in statistical concepts, methods, and techniques
o Develop programs for tables figures and listings
o Develop programs for analysis data sets, including computer-generated table specifications, statistical analysis plan, and research report format
o Develops macros/utilities to increase efficiency
o Communicates with clients regarding statistical analysis issues
o Verify statistical programs, statistical results, and data sets used in statistical section of technical documents
o Responsible for data processing for accurate relocation, formatting, generating and transmitting required data
o May be required to assist in other programming to support data management or specialized data analysis requirements
o Performs quality control procedures on SAS programs
o Mentors other programmers regarding processes, best practices and techniques
o Co-operate in further development of internal manuals and SOPs
o Participate in cross functional meetings and drive initiatives to ensure the delivery of milestones and timelines for clinical trials
o Coordinate technical set-up for complex projects / programs
o Be trained in client SOPs and disseminate knowledge to the SA project team members, as appropriate


This job description does not list all duties of the job. Employees may be asked by supervisors or management to perform other duties.




MINIMUM REQUIREMENTS

o Bachelor’s degree in Statistics, Science or industry-related discipline
o 2 years substantial and related experience in statistics in clinical research
o Ability to apply statistical methodology to well-formulated problems in the clinical research field
o Focus on quality and details
o Analytical expertise in understanding complex issues and their consequences
o Familiar with the application of SAS programming and related systems and software, excellent computer skills and proficient in Microsoft Word, Excel and PowerPoint
o Good communication skills and must be fluent in both written and spoken English or Japanese
o Good team player with excellent interpersonal and organizational skills
o High integrity in personality and professionalism

o Positive attitude, high degree of initiative, committed and able to work independently
o Self-initiative to perform duties, with good analytical and problem-solving capabilities
o Ability to handle multiple tasks and expected to follow through with completion of assigned tasks with minimal supervision
o Meticulous and able to work in a fast-paced environment
o Able to work under pressure and under challenging timelines when required

* ABOUT US

EPS INTERNATIONAL CO., LTD (EPS INTERNATIONAL), a clinical service provider established by a reputable leading full service Japanese contract research organization – EPS Co. Ltd (EPS), commences its operations in 1999 to provide an integrated, seamless and optimal drug development platform through synergizing EPS’s long-established clinical resources and operations in Asia region to best support increasing outsourcing needs in the research, development and commercialization of pharmaceutical products and medical devices initiated by global and Japanese companies worldwide.
 
We have strong presence in Asia and are fast expanding our footprints in the Pacific, Europe and US.
 
Website www.epsgr.com
 
 
* COMPANY VALUES

In line with EPS’s corporate visions, EPS INTERNATIONAL aims to be an “Ever Progressing System” by continuously delivering quality clinical services, providing efficient and effective turn-key solutions for our Clients’ products development needs in Asia region.
 
 
* COMPANY SUCCESS
 
EPS INTERNATIONAL leverages and applies EPS’s values with many years of combined experiences as an added value to our Clients’ programs ranging from research, development to commercialization in key Asian countries. Lead by a great team of professionals with in-depth experiences and relationships supported by regional clinical networks, key opinion leaders and good performance sites, EPS INTERNATIONAL is the preferred outsourcing partner in Asia.

 
One of the large CRO in Japan and listed on Tokyo Nikki Stock Exchange. We are profitable and have strong and stable financial support from EPS Group.


A full service provider from Bioanalytics (Phase I) to Phase IV to Central lab, patient recruitment services, resource solution to meet clients one-stop shop needs


Strong language capabilities within the team - Japanese, Chinese & English. Known as the best Japanese study CRO service provider.

 
Our Data Management Group has a strong brand and reputation in the industry

 
Comparatively large clinical operation team with wide therapeutic area experience that spans over Asia.