Position: Sr. Programmer Analyst
Responsibilities:
Essential
Functions
 Understands and follows department's working practice documents and SOPs,and contribute to their development as needed.
 Understands and follows appropriate corporate SOPs.
 Works directly with project team leaders and client representatives to assess and develop project goals and timelines.
 Independently creates, executes, maintains, and validates programs that transfer data across multiple data management systems or operating systems, combines data from a variety of sources and structures, generates and stores summary data from a variety of sources, generates reports or combines multiple databases.
 Independently creates, executes, maintains, and validates programs that generate listings, tables and figures using SAS.
 Supervises and performs other programming tasks as necessary to support Clinical Data Management and Biostatistics.
 Assesses and ensures the validity of all program output.
 Serves as a project lead and oversees work of other programmers on team.
 Manages assignments to meet timelines and deliver high quality work, being familiar with any relevant contractual obligations or limits.
 Assumes leadership responsibility as a contributing member of a multi-disciplinary clinical trials project team, communicating actively and frequently
with other team members as needed.
 Documents all work; manages assignments to meet timelines and produces high quality deliverables.
 Demonstrates a good understanding of the role of the programmer in the overall process. Increases knowledge base and professional skills in areas including programming, technology and techniques, clinical trials, and the pharmaceutical industry.
 Works efficiently and effectively with little direct supervision.
 Supervises, trains and mentors other programmers.
 Participates in developing SOPs and working practice documents.
 Provides general infrastructure support to the Biostatistics Department. Examples include presentation / teaching at Department meetings, contributing to other general department documents or policies, and assisting with Biostatistics web page development.
 Inputs into bidding process and assists on biostat metrics.
Education and Experience:
MS/MA degree in computer science, statistics, biostatistics, mathematics or related field and a minimum
of three (3) + years experience, or
'Bachelor's degree in computer science, statistics, biostatistics, mathematics or related field or equivalent
and relevant formal academic / vocational qualification, and
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to
5+ years’) or equivalent combination of education, training, & experience.
Position: Statisticians
Responsibilities
• Participate in setting up a study including the development of statistical methodology, fill up the statistical section of study protocol, perform sample size estimation, and carry out randomization procedure
• Develop SAS programs to create statistical tables, listings, and graphics according to the statistical analysis plan
• Perform quality control and/or second program validation of other programmers’ programs.
• Participate in CRF design, review , database setup, data validation and ensure that all critical contents are included
• Develop statistical analysis plan, data validation plan, data management plan and blind data review
• All other duties as assigned
Qualifications:
• Graduate degree in public health, Biostatistics or related disciplines
• At least 1 year experience of statistical analysis in a pharmaceutical or CRO setting
• Excellent communication and interpersonal skills
• Knowledge of ICH GCP and China GCP
• Rich experience of SAS programming, 2 years experience of SAS programming would be preferred
• Being fluent in spoken and written English.
• Be able to work independently and complete a high volume of work
Location: Shanghai & Bei jin
Pls send CV to sarah12087@outlook.com for more detail. |
发表于 2016-11-30 10:50:34