天津招聘

A. Duties and Responsibilities:
Ensure quality of personal work.
Interact with project team members in related disciplines e.g. Clinical Data Management, Clinical and Biostatistics.
Prioritize personal workload to meet specified completion dates.
Display a positive attitude at all times, promoting and contributing to a good team spirit with a productive and professional environment.
Develop good problem solving skills and a willingness to learn and seek advice from senior Statistical Programming staff.
Acquire knowledge of other aspects of the work of a Statistical Programmer Analyst under the supervision of the senior Statistical Programming staff.
Perform other duties as assigned by senior Statistical Programming staff.
Carry out all activities according to Covance SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP).
Develop and review SAS programs and output as required for the management of clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans.
Develop programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of Data Management.
Carry out electronic data transfer (both incoming and outgoing. Develop programs for data transfers and assist in their review to ensure the data transfer has been produced to specification.
Set-up utilities/SAS based systems to assist and facilitate Clinical Data Management activities.
Review draft and final production runs for projects to ensure quality and consistency.

B. Duties and Responsibilities:
Required:
BSc in a computing, life science, mathematical or Statistical subject. A high computing content is considered to be beneficial, however proven computing skills are most important. Alternative academic qualifications or experience are assessed to ensure equivalent background.

C. Experience:
Required:
Some knowledge of SAS and the fundamental principles of programming and program development. Some understanding of the clinical trial process, Data Management and programming activities Good organizational skills and the ability to prioritize own work.
Self motivation. Good time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work. Effective communication skills. A co-operative and team orientated approach. Some general business awareness and an appreciation of the business needs of a CRO.

Pls note: we can consider the candidate who is not in pharma industry but with good experience of SAS, such as the SAS candidate in IT industry is welcomed, pls submit CV to calvin.xu@covance.com thank you!

Covance is one of the world’s largest and most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

Well come to our online job pool to dig out more opportunities at:
http://careers.covance.cn/