Qualifications:         

�          PhD in statistics/biostatistics or other related discipline.

�          4-5 years in the pharmaceutical industry is required.


�          Experience with phase III clinical trial data preferred.

 

Tasks:

Co-develop clinical trial protocols. 
Review, approve, and/or develop statistical analysis plans for clinical trials. 
Oversee implementation, review, and approval of data displays for clinical study reports, NDA
submissions, and other related regulatory documents. 
Maintain all the clinical data collected by CROs and other vendors. 
Analyze clinical data and provide necessary reports in order to support the decision making
process of Chief Scientific Officer. 
Ensure that all activities are done in compliance with regulatory and ICH guidelines. 
 

Please apply online or send resume to [email protected] 

 


About Hudson Scientific
Hudson Scientific provides industry-focused recruitment and contract technical solutions for
the highly specialized scientific arena, specializing in the pharmaceutical, biotechnology and
medical device industries. Hudson responds to the complex dynamics of the scientific
marketplace with industry expertise, targeted recruiting tactics and time-saving solutions. As
such, we have the contacts, expertise and track record to place candidates with leading
employers around the world.