JOIN THE LIFE SCIENCES STAFFING LEADER!
 

TSRI Life Sciences is seeking qualified, experienced professionals at the top of their game who want to make an impact at one of today's global life sciences organizations.  We offer challenging work assignments in a highly energetic, professional workplace. 

 

Our clients are highly regulated thus, we seek candidates with hands on, practical experience with current FDA regulations and a proven track record of successful project work experience. 

 

At TSRI Life Sciences, we are privileged to work with some of the best, highly skilled professionals in the industry and offer a unique work environment for our consultants.  When you work with us, we assess your expertise to gain a greater understanding of your unique abilities.  We keep you up to date on opportunities that match your skills. 

 

Throughout your tenure with us, we keep in constant contact with you and will serve as a strong advocate on your behalf with our clients.  We are deeply committed to your cause and strive to provide you with rewarding, challenging opportunities and the information you need to achieve ultimate success.

 

GREAT REASONS TO JOIN TSRI LIFE SCIENCES

In addition to rewarding assignments, TSRI Life Sciences offers a comprehensive benefits package for our consultants that includes:

  • Medical & Dental Plans

  • Six Paid Holidays

  • 401k Plan

  • Profit Sharing

  • Comprehensive Training & Professional Development

  • Continuing Marketing For Consultants Once Project Is Completed

All candidates must have a successful track record completing project assignments with technologies such as:

EMC/Documentum ISI
QUMAS Extedo
Electronic Publishing Solutions ERM Technologies
Quality Management Systems Clinical Data Management Solutions

 

If you are ready to contribute and have excellent work history, contact us today!
 

REGULATORY SUBMISSION MANAGER - EAST COAST
Excellent opportunity for experienced candidate knowledgeable with eCTD publishing.  Advanced technology experience is a plus.  Seeking candidates with a minimum of 5 years+ experience.
   
SUBMISSION SPECIALIST - MIDWEST & WEST COAST
Seeking experienced candidate for publishing clinical and non-clinical regulatory submission documents in eCTD format.
   
CLINICAL DATA MANAGER - EAST COAST
Thorough understanding of clinical trial methodology, ICH, GCP, and medical terminology.
   
DRUG SAFETY SPECIALIST
Seeking experienced candidate with knowledge of U.S. and non-U.S. regulatory requirements.
   
 
 
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