北京招聘

职位描述：
COMPANY OVERVIEW:
inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 14,000 employees in more than 70 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bio-analytical services, and strategic resourcing from a single clinical professional to an entire functional team.
More information about our company, please visit www.inVentivHealthclinical.com


JOB TITLE: Stat Programmer II/Principal Programmer, Clinical Research
DIVISION: Clinical Research
REPORTS TO: Director , US
LOCATION: Shanghai or Beijing

Key Job Responsibilities:

? Annotate CRFs and review Protocol
? Work closely with Rave database Architect to help develop EDC screens
? Write programs to convert OD to OAD (SDTM-plus) datasets
? Process third party vendor data and edit checks
? Protocol Deviation checks – there are macros that are used in conjunction with additional code to generate protocol deviation checks. Basically, they’re edit checks enveloped under a series of macros.
? Perform validation activities of OD to OAD process
? Process cut-off data using standard macros and the Tosca utilities/panels.
? Work with data manager to establish codelists and develop standard macros
? The setup is aimed at delivering quality data in a timely manner for data analysis and reporting in clinical trial Phase 1 -
? Stats uses the SDTM-plus datasets that the DM programmer generates. Our job is to process all Rave data (i.e. OD) to OAD datasets. Also, all third party vendor data (that I’ve seen) is integrated into the Sdtm-plus datasets
? Incumbent supports study level implementation of medical standards and technical functionality in studies as defined
? Incumbent supports study level implementation of system functionality in close collaboration with Study Managers, Study Lead Monitors, Study Data Managers including DIS study support staff and
? Statistical analysts etc..
? Interact with Bayer (DM Programmer), my Data Manager, Rave database designer, the Statistician, and third party vendors.
? Ensures that study data acquisition setup activities are tested and documented according to applicable SOPs and supports audits and inspections of the same.
? Perform validation on the OD to OAD conversion process.

Required skills:

? Bachelor or advanced degree in statistics, biological sciences, computer science or other equivalent discipline and experience.
? At least 3-5 years relevant experience in clinical research with emphasis in the development and support of the analysis of clinical data.
? Knowledge and experience with international clinical research and drug development.



Candidates who are interested in this opening,
please directly send your CV to Claire Liu: claire.liu@inventivhealth.com 举报 分享

Why Syneos HealthTM? Join a game-changing global company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies - INC Research and inVentiv Health - we bring together more than 21,000 clinical and commercial minds to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.