| Company Information:
Boehringer Ingelheim is currently seeking a talented and innovative Senior Biostatistician to join our Biometrics & Data Management department located at Shanghai, China. As a Biostatistician of Boehringer Ingelheim, you will actively contribute to development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Position Title:
Senior Biostatistician
Duties & Responsibilities:
• To perform duties of a Trial Statistician to support clinical trials within national, regional or international development projects or for marketed products as required. To collaborate with trial team members including Trial Clinical Monitor, pharmacokineticist, etc, in planning clinical protocols conforming to company and regulatory agency guidelines. • To support Project Statisticians in their responsibilities, especially in the planning and preparation of regulatory submissions and contributing to efforts on cross-trial planning and harmonization. • To plan valid, efficient and cost effective clinical trials under Project Statisticians’ guidance and to author Statistical Methodology sections for the protocols and the Trial Statistical Analysis Plans (TSAPs). • To prepare accurate, high quality reports of clinical trials for registration of drugs and biologics, and publications. • To prepare specifications for data analyses by CROs as required. To assure CROs’ compliance with BI SOPs. • To contribute to the development of case report forms and to review for consistency with information needs for the protocol. • To support management in resource planning and tracking for assigned trials.
Position Qualifications:
--- Education & Experience: • Ph.D. in statistics, biostatistics, or biometry with 0-3 years of clinical trial experience in the pharmaceutical industry and/or Regulatory Authorities, or M.S. in the above mentioned areas with at least three years of similar experience. • Ability to design, conduct and analyze a complex trial. • Ability to interact with authorities on statistical issues at the trial level. • Ability to work with project team. • Ability to apply statistical methodology appropriate to drug development. • Ability to communicate basic statistical information to non-statisticians. • Good oral and written communication skills. • Evidence of strong trial teamwork.
Salary Range:
Competitive
Benefits:
Competitive
Web Site:
http://www.boehringer-ingelheim.com.cn/
Application Address:
Luyan Dai
Contact Email: luyan.dai@boehringer-ingelheim.com
Application Deadline:
04/01/2013
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