The Quantitative Decision Strategies group at Janssen Research & Development, 
Johnson & Johnson, is looking for a candidate to represent QDS in Beijing, 
China in the subsidiary company of  Xian-Janssen Pharmacetical Ltd. The basic 
requirements for this candidate are 1) 3+ years experience in a quantitative 
field, but not necessarily pharmaceutical; 2) PhD in statistics or related 
field preferred but not absolutely necessary; 3) speak fluent Chinese and 
English but willing to be located in Beijing; 4) excellent communications 
skill. The full job description follows, if interested, please send resume 
directly to 

Liwei Wang [lwan...@its.jnj.com]

https://jnjc.taleo.net/careersection/2/jobdetail.ftl?lang=en&job=000003XM

====================================================

Senior Quantitative Scientist-000003XM

Description
 
PRINCIPAL RESPONSIBILITIES: List major responsibilities and duties of the 
position. List most complex or difficult parts of job first and indicate 
percentage of time required to perform each task. Describe those quantitative 
aspects of the position which reflect measures that are applicable to the 
position's major responsibilities or end results. (TYPE BELOW THIS LINE)
•       Support for broad implementation of innovative approaches: Implement 
strategy for promoting the broader utilization of innovative approaches across 
the development portfolio, through coordinated efforts involving clinical, 
operational, regulatory areas. Bring together key stakeholders from different 
key areas, identify potential hurdles for broader use of innovation in drug 
development and participate in finding solutions for them. Collaborate in 
talent identification for QDS group, hiring and development. Ensure focus on 
innovation is maintained in QDS group.
 
•       Evaluate and implement innovative approaches: participate in hands-on 
implementation of innovative approaches, through direct interactions with 
clinical teams and other relevant groups. This involves, but is not limited to 
planning, running, and summarizing simulation studies to evaluate the operating 
characteristics of alternative designs and methods; and participating in the 
implementation of the selected approaches by engaging in protocol and SAP 
write-up. Engage external consultants and qualified CROs to provide support in 
the development and implementation of innovative methods, supervising them as 
needed.
 
•       Identification of opportunities for innovation: participate in CDP 
reviews/discussions; interact directly with clinical teams and therapeutic area 
representatives for early identification of opportunities for innovative 
approaches. Assess feasibility and help establish prioritization of identified 
opportunities. Ensure implementation of selected opportunities
 
 
•       Ensuring proper knowledge and awareness of innovative methods and 
designs: help identify, develop, organize, provide and/or arrange training and 
presentations on innovative approaches across the Development organization 
(including statisticians, modelers, clinicians, and other stakeholder groups) 
to ensure awareness and adequate knowledge about these methods. Keep up-to-date 
knowledge of designs and analysis methods for clinical trials, including 
adaptive designs, model-based methods, etc.
 
•       External collaborations, visibility, and impact: engage in external 
collaborations within professional associations, participating  in working 
groups, organizing sessions and presenting at scientific meetings, and 
publishing in peer reviewed journals. Influence the pharmaceutical industry and 
regulatory environments, by engaging in scientific advocacy working groups and 
committees.
 

Qualifications
 
 
•       Doctorate (Ph.D.) in statistics or related field, with a minimum of 3 
years experience in drug development and/or applied quantitative methods for 
decision making, significant knowledge of scientific programming
•       Familiarity with industry principles of drug development, modeling and 
simulation, clinical pharmacology, clinical trial design and regulatory 
guidelines.
•       Sound knowledge of biostatistics applied to clinical trials and 
model-based drug development.
•       Working knowledge of statistical software, such as SAS, R, and S-PLUS, 
WinBugs
•       Have experience with trial simulations to design and document adaptive 
trials and have working knowledge of Bayesian methods.  Stay current with the 
latest statistical methodologies with focus on trial optimization, simulation 
and adaptive designs.
•       Good verbal and written communication skills, including formal 
presentation skills.  Experience presenting to technical and lay groups at 
public meetings desirable.  Written skills as evidenced by publication and 
journal articles also desirable.
•       Ability to successfully multi-task and work independently, under 
minimal supervision; excellent teamwork skills.
•       Ability to influence, negotiate and communicate with both internal and 
external customers.
•       Working knowledge of written and spoken English
•       Knowledge of Good Clinical Practices and regulatory requirements for 
clinical drug development, including the conduct of clinical trials
•       Demonstrated strong CREDO values. Ability to thrive in a global, matrix 
environment.
 
Leadership Skills:  Strong talent identification and development skills,, holds 
self and group fully accountable.
 
Managerial Skills:  Demonstrated strong CREDO values. Ability to thrive in a 
global, matrix environment. Ability to develop, implement and demonstrate 
evidence-based, cost effective and ethical decision making.
 
Technical Skills:  Sound knowledge of statistics, modeling and scientific 
programming. Knowledge of drug development in a global environment. Working 
knowledge of industry principles of drug development, clinical pharmacology, 
clinical trial methodology and regulatory guidelines.
 
Interpersonal Skills:  Good verbal and written communication skills, including 
formal presentation skills.  Experience presenting to technical and lay groups 
at public meetings desirable.  Written skills as evidenced by publication and 
journal articles also desirable.
 
Internal and External Networking Skills:  Ability to successfully manage 
multiple critical issues simultaneously
Ability to negotiate and communicate with both internal and external customers. 
Strategic skills: able to develop, implement, communicate and influence 
strategy internally and externally to the company.

 
Primary Location
 Asia Pacific-China-Beijing-Beijing
Organization
 Xian-Janssen Pharmaceutical Ltd. (7043)
 
 
Job Function
 Clinical Research MD                                     
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