Syntrix Biosystems


 

 
 
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Regulatory affairs & clinical trial management

Syntrix Biosystems is currently seeking an entry level scientist to be part of a team that develops novel therapeutics in the areas of oncology and immunology.

ESSENTIAL DUTIES AND RESPONSIBILITIES: (Other duties may be assigned)

  • Manage ongoing clinical trials, data collection and analysis
  • Develop clinical protocols for new clinical trials either independently or in collaboration with the Company's corporate or academic partners.
  • Assemble and present clinical trial data for submission with a new drug application (NDA) and in compliance with FDA regulations.

KNOWLEDGE, SKILLS AND ABILITIES REQUIRED:

  • M.D. or M.D./Ph.D.
  • Strong background in clinical trial development and management in either an academic or industrial setting.
  • Experience writing and obtaining NIH grant awards highly desired but not absolutely required.
  • Understanding and experience with FDA and other regulatory requirements necessary for bringing a new drug to market.
  • Ability to organize and prioritize tasks in a fast-paced environment with competing deadlines.
  • Strong interpersonal skills to support positive interaction with fellow company members.
  • The ideal candidate will be team oriented and able to work independently.

Syntrix Biosystems offers competitive compensation, comprehensive benefits (including medical, dental and 401k) and the opportunity to be part of a growing team of outstanding scientists.

For consideration, please send your resume to Dr. John A. Zebala at jzebala@syntrixbio.com

We Are An EEO Employer and Value Workplace Diversity

 

 

 

 

 

 

 

Syntrix Biosystems, Inc.

215 Clay Street NW, Suite B-5, Auburn, WA  98001

TEL: 253-833-8009 • FAX: 253-833-8127

 
   
 

email: info@syntrixbio.com

© Copyright 2007 Syntrix Biosystems. All Rights Reserved.